Optically active 1-(fluoro-, trifluoromethyl- or trifluoromethoxy- substituted phenyl)alkylamine N-monoalkyl derivatives and process for producing same

ABSTRACT

An optically active 1-(fluoro-, trifluoromethyl- or trifluoromethoxy-substituted phenyl)alkylamine N-monoalkyl derivative represented by the formula 4 is produced by a process including (a) reacting an optically active secondary amine, represented by the formula 1, with an alkylation agent R 2 —X, in the presence of a base, thereby converting the secondary amine into an optically active tertiary amine represented by the formula 3; and (b) subjecting the tertiary amine to a hydrogenolysis, thereby producing the N-monoalkyl derivative,  
                 
 
     wherein R represents a fluorine atom, trifluoromethyl group or trifluoromethoxy group, n represents an integer of from 1 to 5, each of R 1  and R 2  independently represents an alkyl group having a carbon atom number of from 1 to 6, Me represents a methyl group, Ar represents a phenyl group or 1- or 2-naphthyl group, * represents a chiral carbon, and X represents a leaving group.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a division of co-pending application Ser. No.10/476,650, now U.S. Pat. No. ______, which was the U.S. national stageof international application no. PCT/JP03/11341, filed Sep. 5, 2003, theentire disclosure of which is incorporated herein by reference. Priorityis claimed based on Japanese patent application no. JP 2002-261148,filed Sep. 6, 2002.

BACKGROUND OF THE INVENTION

The present invention relates to (a) optically active 1-(fluoro-,trifluoromethyl-, or trifluoromethoxy-substituted phenyl)alkylamineN-monoalkyl derivatives, which are important intermediates for medicinesand agricultural chemicals, (b) processes for producing thosederivatives, and (c) intermediates, which are obtained in the processes.

Of the above-mentioned N-monoalkyl derivatives, only optically active1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monomethyl is describedin International Publication WO 01/25219, corresponding to U.S. PatentApplication Publication 2003/0028021 A1, and International PublicationWO 02/32867. In fact, WO 01/25219 or U.S. Patent Application Publication2003/0028021 A1 discloses a process for producing optically active1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monomethyl by an opticalresolution of a racemic mixture of1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monomethyl using malicacid.

SUMMARY OF THE INVENTION

It is an object of the present invention to provide a process forproducing optically active 1-(fluoro-, trifluoromethyl-, ortrifluoromethoxy-substituted phenyl)alkylamine N-monoalkyl derivatives.

It is another object of the present invention to provide novel compoundsbelonging to such N-monoalkyl derivatives.

It is still another object of the present invention to provide novelcompounds, which are intermediates obtained in the process.

According to the present invention, there is provided a process forproducing an optically active 1-(fluoro-, trifluoromethyl- ortrifluoromethoxy-substituted phenyl)alkylamine N-monoalkyl derivativerepresented by the formula 4. This process comprises the steps of:

(a) reacting an optically active secondary amine, represented by theformula 1, with an alkylation agent represented by the formula 2, in thepresence of a base, thereby converting the secondary amine into anoptically active tertiary amine represented by the formula 3; and

(b) subjecting the tertiary amine to a hydrogenolysis, thereby producingthe N-monoalkyl derivative,

wherein R represents a fluorine atom, trifluoromethyl group ortrifluoromethoxy group,

n represents an integer of from 1 to 5,

R¹ represents an alkyl group having a carbon atom number of from 1 to 6,

Me represents a methyl group,

Ar represents a phenyl group or 1- or 2-naphthyl group, and

* represents a chiral carbon,R²—X   [2]

wherein R² represents an alkyl group having a carbon atom number of from1 to 6, and X represents a leaving group,

wherein R, n, R¹, Me, Ar, and * are defined as in the formula 1, and R²is defined as in the formula 2,

wherein R, n, R¹, and * are defined as in the formula 1, and R² isdefined as in the formula 2.

According to the present invention, the secondary amine of the abovestep (a) may be produced by a process including the steps of:

(c) reacting a fluoro-, trifluoromethyl- or trifluoromethoxy-substitutedphenyl alkyl ketone, represented by the formula 5, with an opticallyactive primary amine represented by the formula 6 under an acidiccondition to achieve dehydration and condensation, thereby producing anoptically active imine represented by the formula 7; and

(d) asymmetrically reducing the imine by a hydride reducing agent intothe secondary amine,

wherein R, n and R¹ are defined as in the formula 1,

wherein Me, Ar and * are defined as in the formula 1,

wherein R, n, R¹, Me, Ar and * are defined as in the formula 1, and awave line in the formula 7 indicates that the imine is in an Econfiguration or Z configuration.

According to the present invention, there is provided a novel compoundthat is the above tertiary amine represented by the formula 3, which isthe product of the step (a).

According to the present invention, there is provided another novelcompound that is an optically active 1-(fluoro-substitutedphenyl)alkylamine N-monoalkyl derivative represented by the formula 8,

wherein n, R¹ and * are defined as in the formula 1, and R² is definedas in the formula 2.

According to the present invention, there is provided still anothernovel compound that is an optically active1-(trifluoromethyl-substituted phenyl)alkylamine N-monoalkyl derivativerepresented by the formula 9,

wherein n, R¹ and * are defined as in the formula 1, R² is defined as inthe formula 2, and the N-monoalkyl derivative of the formula 9 is acompound except optically active 1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monomethyl.

According to the present invention, there is provided a further novelcompound that is an optically active 1-(trifluoromethoxy-substitutedphenyl)alkylamine N-monoalkyl derivative represented by the formula 10,

wherein n, R¹ and * are defined as in the formula 1, and R² is definedas in the formula 2.

The above novel N-monoalkyl derivatives represented by the formulas 8, 9and 10 correspond to the N-monoalkyl derivative represented by theformula 4, which is the product of the step (b).

DESCRIPTION OF THE PREFERRED EMBODIMENTS

The inventors unexpectedly found that it is possible to efficientlyproduce the target compound, that is, an optically active 1-(fluoro-,trifluoromethyl- or trifluoromethoxy-substituted phenyl) alkylamineN-monoalkyl derivative (represented by the formula 4) with high opticalpurity and high yield by conducting the above process comprising thesteps (a) and (b). Specifically, we unexpectedly found that thehydrogenolysis of the step (b) proceeds selectively on the side of thechiral auxiliary group to sever the N—C* bond only at the broken line“b” in an optically active tertiary amine represented by the followingformula 11 (corresponding to the tertiary amine of the formula 3),although the tertiary amine has two similar α-arylalkyl groupspositioned about the nitrogen atom.

wherein R, n, R¹, Me, Ar, and * are defined as in the formula 1, and R²is defined as in the formula 2. Therefore, it is possible by the step(b) to selectively produce only the target product (i.e., theN-monoalkyl derivative represented by the formula 4).

Furthermore, according to the present invention, the raw material of thestep (a), that is, the optically active secondary amine represented bythe formula 1, can be produced by the above process comprising the stepsof (c) and (d). In other words, the target product of the presentinvention can be produced by a process comprising the sequential stepsof (c), (d), (a) and (b), as shown by the following reaction scheme.

According to the present invention, it is possible to produce the targetcompound of the formula 4 with high optical purity by conducting theabove process comprising the sequential steps of (c), (d), (a) and (b),using an optically active primary amine of the formula 6, which isrelatively low in price, as an asymmetry source.

The dehydration and condensation of the step (c) are described in detailin the following. It is possible to conduct the step (c) by reacting afluoro-, trifluoromethyl- or trifluoromethoxy-substituted phenyl alkylketone, represented by the formula 5, with an optically active primaryamine represented by the formula 6 in the presence of an acid catalyst,thereby producing an optically active imine represented by the formula 7(see the above reaction scheme).

As stated above, R in the formula 5 represents a fluorine atom,trifluoromethyl group or trifluoromethoxy group, and n in the formula 5is an integer of from 1 to 5. Furthermore, each R may take anysubstitution position on the benzene ring of the formula 5. Examples of(R)_(n) of the formula 5 include 2-fluoro, 3-fluoro, 4-fluoro,2,3-difluoro, 2,4-difluoro, 2,5-difluoro, 2,6-difluoro, 3,4-difluoro,3,5-difluoro, 2,3,4-trifluoro, 3,4,5-trifluoro, 2,4,5-trifluoro,2,3,5-trifluoro, 2,3,6-trifluoro, 2,4,6-trifluoro, 2,3,5,6-tetrafluoro,2,4,5,6-tetrafluoro, 3,4,5,6-tetrafluoro, 2,3,4,5,6-pentafluoro,2-trifluoromethyl, 3-trifluoromethyl, 4-trifluoromethyl,2,3-bis(trifluoromethyl), 2,4-bis(trifluoromethyl),2,5-bis(trifluoromethyl), 2,6-bis(trifluoromethyl),3,4-bis(trifluoromethyl), 3,5-bis(trifluoromethyl),2,3,4-tris(trifluoromethyl), 3,4,5-tris(trifluoromethyl),2,4,5-tris(trifluoromethyl), 2,3,5-tris(trifluoromethyl),2,3,6-tris(trifluoromethyl), 2,4,6-tris(trifluoromethyl),2,3,5,6-tetrakis(trifluoromethyl), 2,4,5,6-tetrakis(trifluoromethyl),3,4,5,6-tetrakis(trifluoromethyl), 2,3,4,5,6-pentakis(trifluoromethyl),2- trifluoromethoxy, 3-trifluoromethoxy, 4-trifluoromethoxy,2,3-bis(trifluoromethoxy), 2,4-bis(trifluoromethoxy),2,5-bis(trifluoromethoxy), 2,6-bis(trifluoromethoxy),3,4-bis(trifluoromethoxy), 3,5-bis(trifluoromethoxy),2,3,4-tris(trifluoromethoxy), 3,4,5-tris(trifluoromethoxy),2,4,5-tris(trifluoromethoxy), 2,3,5-tris(trifluoromethoxy),2,3,6-tris(trifluoromethoxy), 2,4,6-tris(trifluoromethoxy),2,3,5,6-tetrakis(trifluoromethoxy), 2,4,5,6-tetrakis(trifluoromethoxy),3,4,5,6-tetrakis(trifluoromethoxy), and2,3,4,5,6-pentakis(trifluoromethoxy).

As stated above, R¹ in the formula 5 represents an alkyl group having acarbon atom number of from 1 to 6. Examples of R¹ include methyl, ethyl,1-propyl, 2-propyl, cyclopropyl, 1-butyl, 2-butyl, 2-methyl-1-propyl,t-butyl, cyclobutyl, 1-pentyl, 2-pentyl, 3-pentyl, neopentyl, t-amyl,cyclopentyl, 1-hexyl, 2-hexyl, 3-hexyl, and cyclohexyl.

Although some of the phenyl alkyl ketones represented by the formula 5are novel compounds depending on the types of (R)_(n) and R¹, they canbe produced, based on the disclosure of Tetrahedron Letters No. 53, pp.4647-4650, 1970.

As stated above, Ar in the formula 6 represents a phenyl, 1-naphthyl or2-naphthyl. Of these, phenyl and 2-naphthyl are preferable, and phenylis more particularly preferable.

The optically active primary amine of the formula 6 may be in Rconfiguration or S configuration in terms of stereochemistry. Either Rconfiguration or S configuration may be used as the raw material of thestep (c) depending on the absolute configuration of the target product.

In the step (c), the primary amine of the formula 6 may have an opticalpurity of not lower than 98% ee (% ee represents enantiomeric excess).

In the step (c), the amount of the primary amine of the formula 6 may beat least one equivalent, preferably 1-10 equivalents, more preferably1-5 equivalents, per equivalent of the phenyl alkyl ketone of theformula 5.

It is possible to use an acid catalyst in the step (c) to make an acidiccondition. The acid catalyst may be selected from organic acids (e.g.,benzenesulfonic acid, p-toluenesulfonic acid, and 10-camphorsulfonicacid) and inorganic acids (e.g., hydrochloric acid, sulfuric acid,phosphoric acid, zinc chloride, and titanium tetrachloride). Of these,p-toluenesulfonic acid, sulfuric acid, and zinc chloride are preferable.In particular, p-toluenesulfonic acid and zinc chloride are morepreferable.

The acid catalyst of the step (c) may be in a catalytic amount,preferably 0.001-0.9 equivalents, more preferably 0.005-0.5 equivalents,per equivalent of the phenyl alkyl ketone of the formula 5.

The step (c) is dehydration and condensation of a phenyl alkyl ketonerepresented by the formula 5 and an optically active primary aminerepresented by the formula 6. Therefore, the reaction can be conductedin the presence of an acid catalyst, while water as a by-product isremoved. It is preferable to conduct the reaction under reflux using asolvent that is immiscible with water, that has a specific gravity lowerthan that of water, and that forms an azeotropic mixture with water,while water as a by-product is removed by a Dean-Stark trap.

The reaction solvent of the step (c) is preferably an aromatichydrocarbon such as benzene, toluene, ethylbenzene, xylene, andmesitylene, particularly preferably toluene. These solvents can be usedalone or in combination.

In the step (c), the reaction solvent is used in an amount such that theamount of water theoretically produced in the reaction can be separatedfrom the reaction liquid as an azeotropic mixture of water and thereaction solvent. It is, however, possible to extremely lower the amountof the reaction solvent by using a Dean-Stark trap.

The reaction of the step (c) can be conducted at a temperature from theazeotrope temperature, at which an azeotropic mixture of water and thereaction solvent is boiled, to the boiling point of the reactionsolvent. It is preferably in the vicinity of the boiling point of thereaction solvent.

Although the reaction of the step (c) may terminate within 120 hr, thereaction time may vary depending on the types of the substrates used andthe reaction conditions. Therefore, it is preferable to terminate thereaction after confirming that the raw material was almost completelyconsumed, by checking the progress of the reaction by a suitableanalytical technique (e.g., gas chromatography, thin layerchromatography, HPLC and NMR).

It is possible to obtain a crude product of the step (c) by conductingan ordinary post-treatment after the reaction. In case that the primaryamine has been used in an excessive amount, it is possible toselectively remove the unreacted primary amine by washing an organiclayer containing an optically active imine of the formula 7 (i.e., theproduct of the step (c)), with an ammonium chloride aqueous solution.According to need, the crude product can be subjected to a purificationsuch as the use of activated carbon, distillation, recrystallization, orcolumn chromatography, thereby obtaining an optically active imine ofthe formula 7 with high chemical purity.

In terms of the double bond geometry, the optically active imine of theformula 7 may be in the form of E geometry or Z geometry. The relativeamounts of these geometries in the resulting imine may change dependingon the reaction substrates used and the reaction conditions.

The step (d) is described in detail in the following. As stated above,the step (d) is conducted by reacting the imine of the formula 7 with ahydride reducing agent.

Since the product of the step (d), an optically active secondary amineof the formula 1, has two stereocenters (chiral carbons), there are fourpossible stereoisomers, R—R configuration, S—R configuration, R—Sconfiguration and S—S configuration, where the letter before the hyphenrepresents the absolute configuration of the 1-(fluoro, trifluoromethylor trifluoromethoxy-substituted phenyl)alkyl group side, and where theletter after the hyphen represents the absolute configuration of theα-arylethyl group (chiral auxiliary agent) side. The four stereoisomersmay be suitably selected depending on the absolute configuration of thetarget product.

A hydride reducing agent to be used in the step (d) can be selected from(1) aluminium hydrides such as (i-Bu)₂AlH, (i-Bu)₃Al,[2,6-(t-Bu)₂-4-Me-Ph]Al(i-Bu)₂, LiAlH₄, LiAlH(OMe)₃, LiAlH(O-t-Bu)₃, andNaAlH₂(OCH₂CH₂OCH₃)₂; (2) boron hydrides such as diborane, BH₃. THF,BH₃. SMe₂, BH₃. NMe₃, 9-BBN, NaBH₄, NaBH₄.CeCl₃, LiBH₄, Zn(BH₄)₂,Ca(BH₄)₂, Lin-BuBH₃, NaBH(OMe)₃, NaBH(OAc)₃, NaBH₃CN, Et₄NBH₄,Me₄NBH(OAc)₃, (n-Bu)₄NBH₃CN, (n-Bu)₄NBH(OAc)₃, Li(s-Bu)₃BH, K(s-Bu)₃BH,LiSia₃BH, KSia₃BH, LiEt₃BH, KPh₃BH, (Ph₃P)₂CuBH₄, ThxBH₂, Sia₂BH,catecholborane, IpcBH₂, and Ipc₂BH; and (3) silicon hydrides such asEt₃SiH, PhMe₂SiH, Ph₂SiH₂, and PhSiH₃.Mo(CO)₆, where Bu represents abutyl group, Ph represents a phenyl group, Me represents a methyl group,THF represents tetrahydrofuran, 9-BBN represents9-borabicyclo[3.3.1]nonane, Ac represents an acetyl group, Siarepresents a thiamyl group, Et represents an ethyl group, Thx representsa thexyl group, and Ipc represents an isopinocampheyl group. Of these,preferable examples are LiAlH₄, diborane, NaBH₄, and LiBH₄. Inparticular, NaBH₄ is more preferable. It is possible to use acombination of at least one of these hydrides and at least one ofvarious inorganic salts.

In the step (d), the hydride reducing agent may be in an amount of 0.25equivalents or greater, preferably 0.25-10 equivalents, more preferably0.25-7 equivalents, per equivalent of the imine of the formula 7.

A reaction solvent usable in the step (d) is not particularly limited.Its examples are (1) aliphatic hydrocarbons such as n-pentane, n-hexane,cyclohexane, and n-heptane; (2) aromatic hydrocarbons such as benzene,toluene, ethylbenzene, xylene, and mesitylene; (3) halogenatedhydrocarbons such as methylene chloride, chloroform, and1,2-dichloroethane; (4) ethers such as diethyl ether, tetrahydrofuran,t-butyl methyl ether, and 1,4-dioxane; (5) esters such as ethyl acetateand n-butyl acetate; (6) nitrites such as acetonitrile andpropionitrile; (7) alcohols such as methanol, ethanol, n-propanol, andi-propanol; and (8) carboxylic acids such as acetic acid, propionicacid, and butyric acid. Of these, preferable examples are diethyl ether,tetrahydrofuran, t-butyl methyl ether, methanol, ethanol, andi-propanol. In particular, tetrahydrofuran, methanol, ethanol, andi-propanol are more preferable. It is possible to use a single solventor a mixture of at least two of these.

The amount of the reaction solvent usable in the step (d) is notparticularly limited. It may be at least one part by volume, preferably1-50 parts by volume, more preferably 1-20 parts by volume, per one partby volume of the imine of the formula 7.

The reaction of the step (d) may be conducted at a temperature of from−100° C. to +100° C., preferably from −80° C. to +80° C., morepreferably from −60° C. to +60° C.

Although the reaction of the step (d) may terminate within 72 hr, thereaction time may vary depending on the types of the substrates used andthe reaction conditions. Therefore, it is preferable to terminate thereaction after confirming that the raw material was almost completelyconsumed, by checking the progress of the reaction by a suitableanalytical technique (e.g., gas chromatography, thin layerchromatography, HPLC and NMR).

It is possible to obtain a crude product of the step (d) by conductingan ordinary post-treatment after the reaction. According to need, thecrude product can be subjected to a purification such as the use ofactivated carbon, distillation, recrystallization, or columnchromatography, thereby obtaining an optically active secondary amine ofthe formula 1 with high chemical purity.

After the step (d), it is possible to improve the secondary amine indiastereomeric excess by a process comprising the steps of:

(e) converting the secondary amine into a salt of an inorganic acid ororganic acid; and

(f) subjecting the salt to a recrystallization.

The inorganic acid of the step (e) may be selected from carbonic acid,hydrochloric acid, sulfuric acid, nitric acid, hydrobromic acid,hydroiodic acid, phosphoric acid, boric acid, perchloric acid, and thelike.

The organic acid of the step (e) may be selected from (1) aliphaticcarboxylic acids such as acetic acid, propionic acid, butyric acid,isobutyric acid, valeric acid, isovaleric acid, hexanoic acid, heptanoicacid, cyclohexanecarboxylic acid, octanoic acid, phenylacetic acid and3-phenylpropionic acid; (2) haloalkylcarboxylic acids such aschloroacetic acid, dichloroacetic acid, trichloroacetic acid,fluoroacetic acid, difluoroacetic acid, trifluoroacetic acid,bromoacetic acid, iodoacetic acid, 2-chloropropionic acid and3-chloropropionic acid; (3) unsaturated carboxylic acids such as acrylicacid, crotonic acid, citraconic acid, maleic acid, fumaric acid and cis-or trans-cinnamic acid; (4) aromatic carboxylic acids such as benzoicacid, o-, m- or p-toluic acid, o-, m- or p-fluorobenzoic acid, o-, m- orp-chlorobenzoic acid, o-, m- or p-bromobenzoic acid, o-, m- orp-iodobenzoic acid, o, m- or p-hydroxybenzoic acid, o-, m- or p-anisicacid, o-, m- or p-aminobenzoic acid, o-, m- or p-nitrobenzoic acid, o-,m- or p-cyanobenzoic acid, m- or p-benzenedicarboxylic acid (phthalicacid, isophthalic acid or terephthalic acid), α-, β- or γ-picolinicacid, 2,6-pyridinedicarboxylic acid and 1- or 2-naphthoic acid; (5)sulfonic acids such as methanesulfonic acid, chloromethanesulfonic acid,trifluoromethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonicacid and p-phenolsulfonic acid; (6) optically active carboxylic acidssuch as lactic acid, malic acid, tartaric acid, dibenzoyltartaric acid,2-phenylpropionic acid, mandelic acid, camphoric acid andcis-2-benzamidocyclohexanecarboxylic acid; (7) optically active sulfonicacids such as phenylethanesulfonic acid and 10-camphorsulfonic acid; (8)optically active phosphoric acids such as2,2′-(1,1′-binaphthyl)phosphoric acid; (9) optically active amino acidssuch as 4-aminobutyric acid, phenylglycine and aspartic acid; (10)optically active N-acylamino acids such as pyroglutamic acid,N-acetyl-3,5-dibromo-tyrosine, N-acyl-phenylalanine, N-acyl-asparticacid, N-acylglutamic acid and N-acylproline (wherein, N-acyl grouprepresents acetyl group, benzyloxycarbonyl group, benzoyl group,benzenesulfonyl group, p-toluenesulfonyl group and the like), and (11)other organic acids such as formic acid, oxalic acid, malonic acid,succinic acid, adipic acid, pimelic acid, cyanoacetic acid, citric acid,glycolic acid, glyoxylic acid, pyruvic acid, levulinic acid, oxaloaceticacid, mercaptoacetic acid, phenoxyacetic acid and picric acid. Althoughthe optically active carboxylic acids, the optically active sulfonicacids, the optically active phosphoric acids, the optically active aminoacids or the optically active N-acylamino acids exist in R configurationor in S configuration, their enantiomers may be suitably selected foruse. Among these, fumaric acid, phthalic acid and p-toluenesulfonic acidare more preferable.

In the step (e), the inorganic or organic acid may be in an amount of0.3 equivalents or greater, preferably 0.3-5 equivalents, morepreferably 0.3-3 equivalents, per equivalent of the secondary amine ofthe formula 1.

The actual operation of the steps (e) and (f) can suitably be selectedin view of the combination of the inorganic or organic acid and theoptically active secondary amine. For example, it is possible to conductthe steps (e) and (f) by directly adding the optically active secondaryamine and an inorganic or organic acid into a recrystallization solvent,followed by mixing. Alternatively, it is possible to mix a solution ofthe optically active secondary amine with a solution of the inorganic ororganic acid to conduct the steps (e) and (f).

The recrystallization solvent of the steps (e) and (f) is notparticularly limited as long as it does not react with the opticallyactive secondary amine, the inorganic or organic acid, and the saltobtained by the step (e). The recrystallization solvent can suitably beselected in view of, for example, (a) the diastereomeric excess prior topurification of the salt using the recrystallization solvent, (b) thediastereomeric excess prior after that, and (c) recovery.

The recrystallization solvent of the steps (e) and (f) may be selectedfrom (1) aliphatic hydrocarbons such as n-pentane, n-hexane, c-hexane,and n-heptane; (2) aromatic hydrocarbons such as benzene, toluene,ethylbenzene, xylene, and mesitylene; (3) halogenated hydrocarbons suchas methylene chloride, chloroform, and 1,2-dichloroethane; (4) etherssuch as diethyl ether, tetrahydrofuran, t-butyl methyl ether, and1,4-dioxane; (5) ketones such as acetone, methyl ethyl ketone, andmethyl isobutyl ketone; (6) esters such as ethyl acetate and n-butylacetate; (7) nitriles such as acetonitrile and propionitrile; (8)alcohols such as methanol, ethanol, n-propanol, i-propanol, andn-butanol; and (9) water. Of these, preferable examples are n-hexane,n-heptane, toluene, methylene chloride, t-butyl methyl ether, acetone,ethyl acetate, acetonitrile, methanol, ethanol, n-propanol, andi-propanol. It is possible to use a single solvent or a mixture of atleast two of these.

The amount of the recrystallization solvent of the steps (e) and (f) isnot particularly limited, as long as the product (salt) of the steps (e)and (f) is completely or partially dissolved therein under heating. Itcan suitably be selected in view of, for example, (a) the diastereomericexcess prior to purification of the salt using the recrystallizationsolvent, (b) the diastereomeric excess after that, and (c) recovery. Forexample, the recrystallization solvent may be in an amount of at least 1part by volume, preferably 1-100 parts by volume, more preferably 1-50parts by volume, relative to the salt of the secondary amine of theformula 1.

Although the secondary amine prior to the steps (e) and (f) is notparticularly limited in diastereomeric excess, it is preferably 10% de(% de represents diastereomeric excess) or greater.

The recrystallization proceeds smoothly and efficiently by adding seedcrystals. The seed crystals are in an amount of preferably from 1/10,000to 1/10 parts by weight, more preferably from 1/5,000 to 1/20 parts byweight, relative to one part by weight of the salt (product) of the step(e) prior to purification.

The temperature for conducting the recrystallization may suitably beselected in view of boiling point and freezing point of therecrystallization solvent. For example, the recrystallization may beconducted by dissolving the salt prior to purification in arecrystallization solvent at a temperature of from room temperature(e.g., 25° C.) to a temperature close to boiling point of therecrystallization solvent and then by precipitating crystals at atemperature of −40 to +80° C.

The precipitated crystals can be recovered by filtration or the like toincrease the diastereomeric excess of the crystals. With this, it ispossible to make the salt (product) of the steps (e) and (f) have highpurity. Its purity can be improved further by repeating therecrystallization operation. The salt itself obtained by the steps (e)and (f) can be used in the alkylation of the step (a). In this case, itsuffices to conduct the alkylation by using a base in an amountsufficient for neutralizing the salt into a free base in the reactionsystem. Alternatively, the salt may be neutralized into a free base tobe used in the step (a). In this case, the salt can be neutralized by aninorganic base aqueous solution, followed by extraction with an organicsolvent. With this, it is possible to efficiently collect the free base.

By conducting the purification of the steps (e) and (f), it is possibleto precipitate crystals of a major isomer contained in the reactionmixture, thereby improving the optical purity. After therecrystallization, the resulting mother liquor may be subjected toprocedures similar to the above recrystallization. With this, a minorisomer may predominantly be crystallized.

The alkylation of the step (a) is described in detail in the following.As stated above, the step (a) is conducted by reacting an opticallyactive secondary amine of the formula 1 with an alkylation agent of theformula 2 in the presence of a base, thereby producing an opticallyactive tertiary amine of the formula 3.

The absolute configurations about the two chiral carbons of thesecondary amine do not change by the alkylation. In other words, thetertiary amine will be in the same stereoisomer (e.g., R—Rconfiguration) as that of the secondary amine.

As stated above, R² in the formula 2 represents an alkyl group having acarbon atom number of from 1 to 6. It may be selected from methyl,ethyl, 1-propyl, 2-propyl, cyclopropyl, 1-butyl, 2-butyl,2-methyl-1-propyl, t-butyl, cyclobutyl, 1-pentyl, 2-pentyl, 3-pentyl,neopentyl, t-amyl, cyclopentyl, 1-hexyl, 2-hexyl, 3-hexyl, cyclohexyland the like.

The leaving group (represented by X) of the alkylation agent may beselected from chlorine, bromine, iodine, mesylate group (MeSO₂O),monochloromesylate group (CH₂ClSO₂O), tosylate group (p-MeC₆H₄SO₂O),triflate group (CF₃SO₂O) and the like. Of these, bromine, iodine,mesylate group, tosylate group, and triflate group are preferable, andbromine, iodine and mesylate group are more preferable.

The amount of the alkylation agent may be at least one equivalent,preferably 1-50 equivalents, 1-30 equivalents, per equivalent of thesecondary amine.

The base used in the step (a) may be selected from (1) organic basessuch as trimethylamine, triethylamine, diisopropylethylamine,tri-n-butylamine, dimethyllaurylamine, dimethylaminopyridine,N,N-dimethylaniline, dimethylbenzylamine,1,8-diazabicyclo[5.4.0]undec-7-ene, 1,4-diazabicyclo[2.2.2]octane,pyridine, 2,4-lutidine, 2,5-lutidine, 2,6-lutidine, 3,4-lutidine,3,5-lutidine, 2,4,6-trimethylpyridine, pyrimidine, and pyridazine; and(2) inorganic bases such as lithium hydride, sodium hydride, potassiumhydride, calcium hydride, lithium carbonate, sodium carbonate, potassiumcarbonate, cesium carbonate, sodium hydrogencarbonate, potassiumhydrogencarbonate, lithium hydroxide, sodium hydroxide, and potassiumhydroxide. Of these, triethylamine, dimethylaminopyridine,1,8-diazabicyclo[5.4.0]undec-7-ene, 2,6-lutidine, sodium hydride, sodiumcarbonate, potassium carbonate, sodium hydrogencarbonate, and potassiumhydrogencarbonate are preferable. In particular, triethylamine,1,8-diazabicyclo[5.4.0]undec-7-ene, 2,6-lutidine, sodium hydride, sodiumcarbonate, and potassium carbonate are more preferable. These bases canbe used alone or in combination.

The amount of the base may be at least one equivalent, preferably 1-50equivalents, more preferably 1-30 equivalents, per equivalent of thesecondary amine.

A reaction solvent usable in the step (a) is not particularly limited.Its examples are (1) aliphatic hydrocarbons such as n-pentane, n-hexane,cyclohexane, and n-heptane; (2) aromatic hydrocarbons such as benzene,toluene, ethylbenzene, xylene, and mesitylene; (3) halogenatedhydrocarbons such as methylene chloride, chloroform, and1,2-dichloroethane; (4) ethers such as diethyl ether, tetrahydrofuran,t-butyl methyl ether, and 1,4-dioxane; (5) esters such as ethyl acetateand n-butyl acetate; (6) amides such as hexamethylphosphoric triamide,N,N-dimethylformamide, N,N-dimethylacetamide, and N-methylpyrolidone.(7) nitriles such as acetonitrile and propionitrile; (8) alcohols suchas methanol, ethanol, n-propanol, and i-propanol; and (9)dimethylsulfoxide. Of these, preferable examples are toluene,1,2-dichloroethane, tetrahydrofuran, ethyl acetate,N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, anddimethylsulfoxide are preferable. In particular, tetrahydrofuran,N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, anddimethylsulfoxide are more preferable. It is possible to use a singlesolvent or a mixture of at least two of these.

The amount of the reaction solvent usable in the step (a) is notparticularly limited. It may be at least one part by volume, preferably1-50 parts by volume, more preferably 1-20 parts by volume, per one partby volume of the secondary amine.

The reaction of the step (a) may be conducted at a temperature of from−10° C. to +200° C., preferably from 0° C. to +175° C., more preferablyfrom +10° C. to +150° C.

Although the reaction of the step (a) may terminate within 72 hr, thereaction time may vary depending on the types of the substrates used andthe reaction conditions. Therefore, it is preferable to terminate thereaction after confirming that the raw material was almost completelyconsumed, by checking the progress of the reaction by a suitableanalytical technique (e.g., gas chromatography, thin layerchromatography, HPLC and NMR).

It is possible to obtain a crude product of the step (a) by conductingan ordinary post-treatment after the reaction. According to need, thecrude product can be subjected to a purification such as the use ofactivated carbon, distillation, recrystallization, or columnchromatography, thereby obtaining an optically active tertiary amine ofthe formula 3 with high chemical purity.

The hydrogenolysis of the step (b) is described in detail in thefollowing. The hydrogenolysis is achieved by reacting the tertiary aminewith hydrogen, thereby producing the target product of the presentinvention, the N-monoalkyl derivative of the formula 4.

In case that the tertiary amine is in the R—R configuration or R—Sconfiguration, R configuration becomes excessive in the product of thestep (b). In case that the tertiary amine is in the S—S configuration orS—R configuration, S configuration becomes excessive in the product ofthe step (b).

The hydrogenolysis can proceed well by a catalytic reduction using atransition metal complex as a catalyst. This transition metal complexcan be selected from (1) platinum catalysts such as platinum oxide,platinum/active carbon and platinum black; (2) nickel catalysts such asreduced nickel, Raney nickel and platinum-Raney nickel; (3) cobaltcatalysts such as Raney cobalt; (4) ruthenium catalysts such asruthenium oxide and ruthenium/active carbon; (5) rhodium catalysts suchas rhodium/active carbon, rhodium/alumina and rhodium-platinum oxide;(6) iridium catalysts such as iridium black; and (7) palladium catalystssuch as palladium/active carbon, palladium hydroxide, palladium black,palladium/barium sulfate, palladium/strontium carbonate,palladium/calcium carbonate, palladium/calcium carbonate-lead diacetate,palladium/barium sulfate-quinoline, palladium/alumina, palladium sponge,palladium chloride, palladium acetate, palladium acetylacetonate,bis(dibenzylideneacetone)palladium,tetrakis(triphenylphosphine)palladium,dichloro[bis(triphenylphosphine)]palladium,dichloro[bis(diphenylphosphino)methane]palladium,dichloro[bis(diphenylphosphino)ethane]palladium,dichloro[1,3-bis(diphenylphosphino)propane]palladium,dichloro[1,4-bis(diphenylphosphino)butane]palladium, dichloro(1,5-cyclooctadiene)palladium, dichloro[bis(benzonitrile)]palladium,dichloro[bis(acetonitrile)]palladium, and[bis(triphenylphosphine)]palladium acetate. Among these, platinumcatalysts, rhodium catalysts and palladium catalysts are preferable, andplatinum/active carbon, rhodium/active carbon and palladium/activecarbon are particularly more preferable. These catalysts can be usedalone or in combination. In the case of using a catalyst in which ametal is loaded onto a support, the loaded amount is 0.1-50 wt %,preferably 0.5-30 wt %, and particularly more preferably 1-20 wt %. Inaddition, in order to enhance safety during handling or to preventoxidation of the metal surface, it is possible to use a transition metalcomplex stored in water or mineral oil.

The transition metal complex (in terms of metal contained in thecomplex) may be in an amount of 0.5 wt % or less, preferably 0.001-0.4wt %, more preferably 0.005-0.3 wt %, based on the total weight (100 wt%) of the tertiary amine.

The hydrogenolysis of the step (b) may be conducted by using hydrogen inan amount of at least one equivalent, per equivalent of the tertiaryamine. It is, however, usual to use hydrogen excessively due to thehydrogenolysis under a hydrogen atmosphere. The hydrogen pressure may be2 MPa or less, preferably 0.01-1.5 MPa, more preferably 0.05-1.0 MPa.

The hydrogenolysis can proceed smoothly by adding an organic orinorganic acid as an additive. Its examples include organic acids suchas acetic acid, propionic acid, butyric acid, p-toluenesulfonic acid,and 10-camphorsulfonic acid; and inorganic acids such as hydrochloricacid, sulfuric acid, nitric acid, hydrobromic acid, and hydroiodic acid.Of these, acetic acid, propionic acid, hydrochloric acid, sulfuric acid,and hydrobromic acid are preferable, and acetic acid, hydrochloric acidand sulfuric acid are more preferable.

The additive of the hydrogenolysis may be in an amount of 0.1equivalents or more, preferably 0.1-100 equivalents, more preferably0.1-50 equivalents, per equivalent of the tertiary amine.

The reaction solvent usable in the step (b) may be selected from (1)aliphatic hydrocarbons such as n-pentane, n-hexane, c-hexane, andn-heptane; (2) aromatic hydrocarbons such as benzene, toluene,ethylbenzene, xylene, and mesitylene; (3) ethers such as diethyl ether,tetrahydrofuran, t-butyl methyl ether, and 1,4-dioxane; (4) esters suchas ethyl acetate and n-butyl acetate; (5) alcohols such as methanol,ethanol, n-propanol, and i-propanol; (6) carboxylic acids such as aceticacid, propionic acid, and butyric acid; (7) acidic aqueous solutionssuch as hydrochloric acid, sulfuric acid, hydrobromic acid,p-toluenesulfonic acid and 10-camphorsulfonic acid; and (8) water. Amongthese, toluene, ethyl acetate, methanol, ethanol, i-propanol, aceticacid and hydrochloric acid aqueous solution are preferable, whilemethanol, ethanol, i-propanol, acetic acid and hydrochloric acid aqueoussolution are particularly more preferable. These reaction solvents canbe used alone or in combination.

The amount of the reaction solvent usable in the hydrogenolysis is notparticularly limited. It may be at least one part by volume, preferably1-100 parts by volume, more preferably 1-50 parts by volume, per onevolume of the tertiary amine.

The hydrogenolysis may be conducted at a temperature of +40° C. orhigher, preferably +40° C. to +200° C., more preferably +40° C. to +150°C.

Although the reaction of the step (b) may terminate within 72 hr, thereaction time may vary depending on the types of the substrates used andthe reaction conditions. Therefore, it is preferable to terminate thereaction after confirming that the raw material was almost completelyconsumed, by checking the progress of the reaction by a suitableanalytical technique (e.g., gas chromatography, thin layerchromatography, HPLC and NMR).

It is possible to obtain a crude product of the step (b) by conductingan ordinary post-treatment after the reaction. In case that an organicor inorganic acid has been added as the additive in the step (b), it ispossible to efficiently collect the target free base by neutralizing thereaction mixture with an inorganic base aqueous solution, followed byextraction with an organic solvent. According to need, the crude productcan be subjected to a purification such as the use of activated carbon,distillation, recrystallization, or column chromatography, therebyobtaining an optically active 1-(fluoro-, trifluoromethyl- ortrifluoromethoxy-substituted phenyl)alkylamine N-monoalkyl derivative ofthe formula 4 with high optical purity and high chemical purity.

Nonlimitative examples of the target product represented by the formula4, which can be produced by the present invention, include(R)-1-(2-fluorophenyl)ethylamine N-monomethyl,(S)-1-(2-fluorophenyl)ethylamine N-monomethyl,(R)-1-(3-fluorophenyl)ethylamine N-monomethyl,(S)-1-(3-fluorophenyl)ethylamine N-monomethyl,(R)-1-(4-fluorophenyl)ethylamine N-monomethyl,(S)-1-(4-fluorophenyl)ethylamine N-monomethyl,(R)-1-(3,5-difluorophenyl)ethylamine N-monomethyl,(S)-1-(3,5-difluorophenyl)ethylamine N-monomethyl,(R)-1-(2-fluorophenyl)propylamine N-monomethyl,(S)-1-(2-fluorophenyl)propylamine N-monomethyl,(R)-1-(3-fluorophenyl)propylamine N-monomethyl,(S)-1-(3-fluorophenyl)propylamine N-monomethyl,(R)-1-(4-fluorophenyl)propylamine N-monomethyl,(S)-1-(4-fluorophenyl)propylamine N-monomethyl, (R)1-(3,5-difluorophenyl)propylamine N-monomethyl,(S)-1-(3,5-difluorophenyl)propylamine N-monomethyl,(R)-1-(2-fluorophenyl)pentylamine N-monomethyl,(S)-1-(2-fluorophenyl)pentylamine N-monomethyl,(R)-1-(3-fluorophenyl)pentylamine N-monomethyl,(S)-1-(3-fluorophenyl)pentylamine N-monomethyl,(R)-1-(4-fluorophenyl)pentylamine N-monomethyl, (S)-1-(4-fluorophenyl)pentylamine N-monomethyl,(R)-1-(3,5-difluorophenyl)pentylamine N-monomethyl,(S)-1-(3,5-difluorophenyl)pentylamine N-monomethyl,(R)-1-(2-fluorophenyl)ethylamine N-monoethyl,(S)-1-(2-fluorophenyl)ethylamine N-monoethyl,(R)-1-(3-fluorophenyl)ethylamine N-monoethyl,(S)-1-(3-fluorophenyl)ethylamine N-monoethyl,(R)-1-(4-fluorophenyl)ethylamine N-monoethyl,(S)-1-(4-fluorophenyl)ethylamine N-monoethyl, (R)-1-(3,5-difluorophenyl)ethylamine N-monoethyl,(S)-1-(3,5-difluorophenyl)ethylamine N-monoethyl,(R)-1-(2-fluorophenyl)propylamine N-monoethyl,(S)-1-(2-fluorophenyl)propylamine N-monoethyl,(R)-1-(3-fluorophenyl)propylamine N-monoethyl,(S)-1-(3-fluorophenyl)propylamine N-monoethyl,(R)-1-(4-fluorophenyl)propylamine N-monoethyl,(S)-1-(4-fluorophenyl)propylamine N-monoethyl,(R)-1-(3,5-difluorophenyl)propylamine N-monoethyl, (S)-1-(3,5-difluorophenyl)propylamine N-monoethyl,(R)-1-(2-fluorophenyl)pentylamine N-monoethyl,(S)-1-(2-fluorophenyl)pentylamine N-monoethyl,(R)-1-(3-fluorophenyl)pentylamine N-monoethyl,(S)-1-(3-fluorophenyl)pentylamine N-monoethyl,(R)-1-(4-fluorophenyl)pentylamine N-monoethyl,(S)-1-(4-fluorophenyl)pentylamine N-monoethyl, (R)1-(3,5-difluorophenyl)pentylamine N-monoethyl,(S)-1-(3,5-difluorophenyl)pentylamine N-monoethyl,(R)-1-(2-trifluoromethylphenyl)ethylamine N-monomethyl,(S)-1-(2-trifluoromethylphenyl)ethylamine N-monomethyl,(R)-1-(3-trifluoromethylphenyl)ethylamine N-monomethyl,(S)-1-(3-trifluoromethylphenyl)ethylamine N-monomethyl,(R)-1-(4-trifluoromethylphenyl)ethylamine N-monomethyl, (S)-1-(4-trifluoromethylphenyl)ethylamine N-monomethyl,(R)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monomethyl,(S)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monomethyl,(R)-1-(2-trifluoromethylphenyl)propylamine N-monomethyl,(S)-1-(2-trifluoromethylphenyl)propylamine N-monomethyl,(R)-1-(3-trifluoromethylphenyl)propylamine N-monomethyl,(S)-1-(3-trifluoromethylphenyl)propylamine N-monomethyl,(R)-1-(4-trifluoromethylphenyl)propylamine N-monomethyl,(S)-1-(4-trifluoromethylphenyl)propylamine N-monomethyl,(R)-1-(3,5-bis(trifluoromethyl)phenyl)propylamine N-monomethyl,(S)-1-(3,5-bis(trifluoromethyl)phenyl)propylamine N-monomethyl,(R)-1-(2-trifluoromethylphenyl)pentylamine N-monomethyl,(S)-1-(2-trifluoromethylphenyl)pentylamine N-monomethyl,(R)-1-(3-trifluoromethylphenyl)pentylamine N-monomethyl,(S)-1-(3-trifluoromethylplienyl)pentylamine N-monomethyl,(R)-1-(4-trifluoromethylphenyl)pentylamine N-monomethyl,(S)-1-(4-trifluoromethylphenyl)pentylamine N-monomethyl,(R)-1-(3,5-bis(trifluoromethyl)phenyl)pentylamine N-monomethyl,(S)-1-(3,5-bis(trifluoromethyl)phenyl)pentylamine N-monomethyl,(R)-1-(2-trifluoromethylphenyl)ethylamine N-monoethyl,(S)-1-(2-trifluoromethylphenyl)ethylamine N-monoethyl,(R)-1-(3-trifluoromethylphenyl)ethylamine N-monoethyl,(S)-1-(3-trifluoromethylphenyl)ethylamine N-monoethyl,(R)-1-(4-trifluoromethylphenyl)ethylamine N-monoethyl,(S)-1-(4-trifluoromethylphenyl)ethylamine N-monoethyl,(R)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monoethyl,(S)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monoethyl,(R)-1-(2-trifluoromethylphenyl)propylamine N-monoethyl,(S)-1-(2-trifluoromethylphenyl)propylamine N-monoethyl,(R)-1-(3-trifluoromethylphenyl)propylamine N-monoethyl,(S)-1-(3-trifluoromethylphenyl)propylamine N-monoethyl,(R)-1-(4-trifluoromethylphenyl)propylamine N-monoethyl,(S)-1-(4-trifluoromethylphenyl)propylamine N-monoethyl,(R)-1-(3,5-bis(trifluoromethyl)phenyl)propylamine N-monoethyl,(S)-1-(3,5-bis(trifluoromethyl)phenyl)propylamine N-monoethyl,(R)-1-(2-trifluoromethylphenyl)pentylamine N-monoethyl,(S)-1-(2-trifluoromethylphenyl)pentylamine N-monoethyl,(R)-1-(3-trifluoromethylphenyl)pentylamine N-monoethyl,(S)-1-(3-trifluoromethylphenyl)pentylamine N-monoethyl,(R)-1-(4-trifluoromethylphenyl)pentylamine N-monoethyl,(S)-1-(4-trifluoromethylphenyl)pentylamine N-monoethyl,(R)-1-(3,5-bis(trifluoromethyl)phenyl)pentylamine N-monoethyl,(S)-1-(3,5-bis(trifluoromethyl)phenyl)pentylamine N-monoethyl,(R)-1-(2-trifluoromethoxyphenyl)ethylamine N-monomethyl,(S)-1-(2-trifluoromethoxyphenyl)ethylamine N-monomethyl,(R)-1-(3-trifluoromethoxyphenyl)ethylamine N-monomethyl,(S)-1-(3-trifluoromethoxyphenyl)ethylamine N-monomethyl,(R)-1-(4-trifluoromethoxyphenyl)ethylamine N-monomethyl,(S)-1-(4-trifluoromethoxyphenyl)ethylamine N-monomethyl,(R)-1-(3,5-bis(trifluoromethoxy)phenyl)ethylamine N-monomethyl,(S)-1-(3,5-bis(trifluoromethoxy)phenyl)ethylamine N-monomethyl,(R)-1-(2-trifluoromethoxyphenyl)propylamine N-monomethyl,(S)-1-(2-trifluoromethoxyphenyl)propylamine N-monomethyl,(R)-1-(3-trifluoromethoxyphenyl)propylamine N-monomethyl,(S)-1-(3-trifluoromethoxyphenyl)propylamine N-monomethyl,(R)-1-(4-trifluoromethoxyphenyl)propylamine N-monomethyl,(S)-1-(4-trifluoromethoxyphenyl)propylamine N-monomethyl, (R)1-(3,5-bis(trifluoromethoxy)phenyl)propylamine N-monomethyl,(S)-1-(3,5-bis(trifluoromethoxy)phenyl)propylamine N-monomethyl,(R)-1-(2-trifluoromethoxyphenyl)pentylamine N-monomethyl,(S)-1-(2-trifluoromethoxyphenyl)pentylamine N-monomethyl,(R)-1-(3-trifluoromethoxyphenyl)pentylamine N-monomethyl,(S)-1(3-trifluoromethoxyphenyl)pentylamine N-monomethyl,(R)-1-(4-trifluoromethoxyphenyl)pentylamine N-monomethyl,(S)-1-(4-trifluoromethoxyphenyl)pentylamine N-monomethyl,(R)-1-(3,5-bis(trifluoromethoxy)phenyl)pentylamine N-monomethyl,(S)-1-(3,5-bis(trifluoromethoxy)phenyl)pentylamine N-monomethyl,(R)-1-(2-trifluoromethoxyphenyl)ethylamine N-monoethyl,(S)-1-(2-trifluoromethoxyphenyl)ethylamine N-monoethyl,(R)-1-(3-trifluoromethoxyphenyl)ethylamine N-monoethyl,(S)-1-(3-trifluoromethoxyphenyl)ethylamine N-monoethyl,(R)-1-(4-trifluoromethoxyphenyl)ethylamine N-monoethyl,(S)-1-(4-trifluoromethoxyphenyl)ethylamine N-monoethyl,(R)-1-(3,5-bis(trifluoromethoxy)phenyl)ethylamine N-monoethyl,(S)-1-(3,5-bis(trifluoromethoxy)phenyl)ethylamine N-monoethyl,(R)-1-(2-trifluoromethoxyphenyl)propylamine N-monoethyl,(S)-1-(2-trifluoromethoxyphenyl)propylamine N-monoethyl,(R)-1-(3-trifluoromethoxyphenyl)propylamine N-monoethyl,(S)-1-(3-trifluoromethoxyphenyl)propylamine N-monoethyl,(R)-1-(4-trifluoromethoxyphenyl)propylamine N-monoethyl,(S)-1-(4-trifluoromethoxyphenyl)propylamine N-monoethyl,(R)-1-(3,5-bis(trifluoromethoxy)phenyl)propylamine N-monoethyl,(S)-1-(3,5-bis(trifluoromethoxy)phenyl)propylamine N-monoethyl,(R)-1-(2-trifluoromethoxyphenyl)pentylamine N-monoethyl,(S)-1-(2-trifluoromethoxyphenyl)pentylamine N-monoethyl,(R)-1-(3-trifluoromethoxyphenyl)pentylamine N-monoethyl,(S)-1-(3-trifluoromethoxyphenyl)pentylamine N-monoethyl,(R)-1-(4-trifluoromethoxyphenyl)pentylamine N-monoethyl, (S)-1-(4-trifluoromethoxyphenyl)pentylamine N-monoethyl,(R)-1-(3,5-bis(trifluoromethoxy)phenyl)pentylamine N-monoethyl, and(S)-1-(3,5-bis(trifluoromethoxy)phenyl)pentylamine N-monoethyl.

The following nonlimitative examples are illustrative of the presentinvention.

EXAMPLE 1 SYNTHESIS OF OPTICALLY ACTIVE (S)-1-(4-FLUOROPHENYL)ETHYLAMINEN-MONOMETHYL Step (c), dehydration and condensation

At first, 20.00 g (144.78 mmol, 1 eq.) of 4-fluorophenyl methyl ketone,19.30 g (159.27 mmol, 1.10 eq.) of (S)-1-phenylethylamine, and 0.60 g(4.40 mmol, 0.03 eq.) of zinc chloride were added to 145 ml of toluene.The resulting mixture was stirred for 19 hr under a heated refluxcondition, while water (by-product) was removed from a Dean-Stark trap.The resulting reaction liquid was washed with 5% sodium hydroxideaqueous solution, 1.5N ammonium chloride aqueous solution, and water.The recovered organic layer was dried with anhydrous sodium sulfate,filtrated, concentrated and vacuum-dried, thereby obtaining 35.00 g of acrude product of an optically active imine represented by the followingformula.

Conversion was found by gas chromatography to be 98%.

¹H-NMR (standard substance: TMS; solvent: CDCl₃), δppm: 1.53 (d, 6.6 Hz,3H), 2.25 (s, 3H), 4.82 (q, 6.6 Hz, 1H), 7.00-7.50 (Ar—H, 7H), 7.80-7.90(Ar—H, 2H).

Step (d), Asymmetric Reduction

At first, 35.00 g (144.78 mmol, 1 eq.) of the crude product of theoptically active imine produced by the above step (c) were added to 120ml of methanol. The resulting solution was cooled down to 0° C. Then,5.50 g (145.39 mmol, 1.00 eq.) of sodium borohydride were added,followed by stirring for 5 hr at the same temperature. After thereaction, 1N hydrochloric acid aqueous solution was added to decomposethe remaining sodium borohydride. Then, the reaction liquid was madebasic by adding 1N sodium hydroxide aqueous solution, followed byextraction with toluene. The collected organic layer was washed withwater, dried with anhydrous sodium sulfate, filtrated, concentrated, andvacuum-dried, thereby obtaining 35.34 g of a crude product of anoptically active secondary amine represented by the following formula.

It was found by gas chromatography that conversion of the crude productwas 100% and that the ratio of a diastereomer of S—S configuration to adiastereomer of R—S configuration was 93:7.

The NMR data of the crude product are as follows.

¹H-NMR (TMS, CDCl₃) of S—S configuration, δppm: 1.24 (d, 6.4 Hz, 3H),1.27 (d, 6.4 Hz, 3H), 1.60 (br, 1H), 3.45 (q, 6.4 Hz, 1H), 3.49 (q, 6.4Hz, 1H), 6.90-7.50 (Ar—H, 9H).

¹H-NMR (TMS, CDCl₃) of R—S configuration, δppm: 1.32 (d, 6.8 Hz, 3H),1.35 (d, 6.8 Hz, 3H), 1.60 (br, 1H), 3.74 (q, 6.8 Hz, 2H), 6.90-7.50(Ar—H, 9H)

Steps (e) and (f), Salt Formation and its Recrystallization

8.00 g (32.77 mmol, 1 eq.) of the crude product of the optically activesecondary amine produced by the above step (d) and 5.44 g (32.75 mmol,1.00 eq.) of phthalic acid were added to 39.5 ml of i-propanol, followedby dissolving these solutes at 50° C. The resulting solution was allowedto cool down to room temperature, followed by addition of seed crystalsand then stirring for 12 hr. The precipitated crystals were filtered,washed with a small amount of n-heptane, and vacuum-dried, therebyobtaining 10.06 g of crystals of a phthalate of the optically activesecondary amine, which is represented by the following formula.

The diastereomeric excess of the crystals was determined by gaschromatography in a manner that the phthalate was turned into a freebase with 1N sodium hydroxide aqueous solution. The result was 99.3% de.The total yield from the dehydration and the condensation to the saltformation and its recrystallization was 75%.

¹H-NMR (TMS, CDCl₃), δppm: 1.78 (d, 6.8 Hz, 6H), 4.03 (q, 6.8 Hz, 1H),4.06 (q, 6.8 Hz, 1H), 7.09 (Ar—H, 2H), 7.36-7.48 (Ar—H, 7H), 7.55-7.65(Ar—H, 2H), 8.45-8.55 (Ar—H, 2H), 10.40 (br, 3H).

Then, 1N sodium hydroxide aqueous solution was added to 6.70 g (16.36mmol) of the crystals of the phthalate to have a basic solution,followed by extraction with toluene. The collected organic layer waswashed with water and then saturated brine, dried with anhydrous sodiumsulfate, filtrated, concentrated, and vacuum-dried, thereby obtaining3.98 g of a purified product of an optically active secondary aminerepresented by the following formula.

The recovery was quantitative.

¹H-NMR (TMS, CDCl₃), δppm: 1.24 (d, 6.4 Hz, 3H), 1.27 (d, 6.4 Hz, 3H),1.60 (br, 1H), 3.45 (q, 6.4 Hz, 1H), 3.49 (q, 6.4 Hz, 1H), 6.90-7.50(Ar—H, 9H).

Step (a), Alkylation

At first, 1.50 g (6.16 mmol, 1 eq.) of the above purified product of theoptically active secondary amine, 4.38 g (30.86 mmol, 5.01 eq.) ofmethyl iodide, and 1.70 g (12.30 mmol, 2.00 eq.) of anhydrous potassiumcarbonate were added to a mixed solution of 0.6 ml of dimethylformamideand 5.6 ml of tetrahydrofuran, followed by stirring at 45-50° C. for 24hr. After the reaction, the reaction liquid was diluted with ethylacetate, followed by washing with saturated brine, drying with anhydroussodium sulfate, filtration, concentration, and vacuum drying, therebyobtaining 1.99 g of a crude product of an optically active tertiaryamine represented by the following formula.

Conversion was found by gas chromatography to be 100%. Furthermore, thecrude product was purified by a silica gel column chromatography (ethylacetate : n-hexane=1:10), thereby obtaining 1.38 g of a purified productof the optically active tertiary amine. The yield was 87%.

¹H-NMR (TMS, CDCl₃), δppm: 1.23 (d, 6.8 Hz, 3H), 1.25 (d, 6.8 Hz, 3H),1.90 (s, 3H), 3.71 (q, 6.8 Hz, 1H), 3.74 (q, 6.8 Hz, 1H), 6.93 (Ar—H,2H), 7.12-7.32 (Ar—H, 7H).

Step (b), Hydrogenolysis

To 2.7 ml of methanol, 0.70 g (2.72 mmol, 1 eq.) of the above purifiedproduct of the optically active tertiary amine, 0.81 g (13.49 mmol, 4.96eq.) of acetic acid, and 34.8 mg (0.124 wt % Pd, based on the totalweight of the tertiary amine) of a palladium catalyst (having 5%palladium carried on an activated carbon containing 50 wt % of water)were added. The hydrogen pressure was adjusted to 0.6 MPa, and thestirring was conducted at 65° C. for 40 hr. After the reaction, thereaction liquid was filtrated using a filtration aid (CELITE (tradename)), concentrated, and vacuum-dried, thereby obtaining a crudeproduct of an acetate of an optically active(S)-1-(4-fluorophenyl)ethylamine N-monomethyl, represented by thefollowing formula.

Then, 1N sodium hydroxide aqueous solution was added to the above crudeproduct of the acetate to have a basic solution, followed by extractionwith ethyl acetate. The recovered organic layer was dried with anhydroussodium sulfate, followed by filtration, concentration, and vacuumdrying, thereby obtaining 0.35 g of a crude product of an opticallyactive (S)-1-(4-fluorophenyl)ethylamine N-monomethyl represented by thefollowing formula.

The yield was 83%. The above crude product was found by chiral gaschromatography to have a conversion of 99% and an enantiomeric excess of99.3% ee. In terms of severing position selectivity whether the N—C*bond is severed at the broken line “a” to produce a compound A or at thebroken line “b” to produce a compound B (i.e., the above opticallyactive (S)-1-(4-fluorophenyl)ethylamine N-monomethyl) in the aboveformula 11, the above crude product was found by chiral gaschromatography to contain 1 part by mole of the compound A and 99 partsby mole of the compound B.

¹H-NMR (TMS, CDCl₃), δppm: 1.33 (d, 6.4 Hz, 3H), 1.65 (br, 1H), 2.29 (s,3H), 3.64 (q, 6.4 Hz, 1H), 7.01 (Ar—H, 2H), 7.26 (Ar—H, 2H).

EXAMPLE 2 SYNTHESIS OF OPTICALLY ACTIVE (R)-1-(4-FLUOROPHENYL)ETHYLAMINEN-MONOMETHYL

Example 1 was repeated except in that (S)-1-phenylethylamine wasreplaced with (R)-1-phenylethylamine, thereby obtaining an opticallyactive (R)-1-(4-fluorophenyl)ethylamine N-monomethyl.

NMR data of an optically active tertiary amine, represented by thefollowing formula, are shown as follows.

¹H-NMR (TMS, CDCl₃), δppm: 1.23 (d, 6.8 Hz, 3H), 1.25 (d, 6.8 Hz, 3H),1.90 (s, 3H), 3.71 (q, 6.8 Hz, 1H), 3.74 (q, 6.8 Hz, 1H), 6.93 (Ar—H,2H), 7.12-7.32 (Ar—H, 7H).

NMR data of an optically active (R)-1-(4-fluorophenyl)ethylamineN-monomethyl, represented by the following formula, are shown asfollows.

¹H-NMR (TMS, CDCl₃), δppm: 1.33 (d, 6.4 Hz, 3H), 1.65 (br, 1H), 2.29 (s,3H), 3.64 (q, 6.4 Hz, 1H), 7.01 (Ar—H, 2H), 7.26 (Ar—H, 2H).

In chiral gas chromatography, the major enantiomer peaks of Example 2were identical with the minor enantiomer peaks of Example 1, and theminor enantiomer peaks of Example 2 were identical with the majorenantiomer peaks of Example 1.

EXAMPLE 3 OPTICALLY ACTIVE (S)-1-(4-FLUOROPHENYL)PROPYLAMINEN-MONOMETHYL Step (c), Dehydration and Condensation

At first, 45.65 g (299.99 mmol, 1 eq.) of 4-fluorophenyl ethyl ketone,39.99 g (330.00 mmol, 1.10 eq.) of (S)-1-phenylethylamine, and 3.27 g(23.99 mmol, 0.08 eq.) of zinc chloride were added to 300 ml of toluene.The resulting mixture was stirred for 42 hr under a heated refluxcondition, while water (by-product) was removed from a Dean-Stark trap.The resulting reaction liquid was washed with 5% sodium hydroxideaqueous solution, 1.5N ammonium chloride aqueous solution, and water.The recovered organic layer was dried with anhydrous sodium sulfate,filtrated, concentrated and vacuum-dried, thereby obtaining 79.20 g of acrude product of an optically active imine represented by the followingformula.

Conversion was found by gas chromatography to be 94%. The molecularratio of E configuration to Z configuration of the crude product wasfound by 1H-NMR to be 75:25.

¹H-NMR (standard substance: TMS; solvent: CDCl₃) of E configuration,δppm: 1.05 (t, 7.8 Hz, 3H), 1.54 (d, 6.6 Hz, 3H), 2.73 (m, 2H), 4.87 (q,6.6 Hz 1H), 6.90-7.90 (Ar—H, 9H).

¹H-NMR (standard substance: TMS; solvent: CDCl₃) of Z configuration,δppm: 1.09 (t, 7.6 Hz, 3H), 1.38 (d, 6.6 Hz, 3H), 2.56 (m, 2H), 4.36 (q,6.6 Hz 1H), 6.90-7.90 (Ar—H, 9H).

Step (d), Asymmetric Reduction

At first, 79.20 g (299.99 mmol, 1 eq.) of the crude product of theoptically active imine produced by the above step (c) were added to 390ml of methanol. The resulting solution was cooled down to 0° C. Then,11.35 g (300.03 mmol, 1.00 eq.) of sodium borohydride were added,followed by stirring for 3 hr at the same temperature. After thereaction, 1N hydrochloric acid aqueous solution was added to decomposethe remaining sodium borohydride. Then, the reaction liquid was madebasic by adding 1N sodium hydroxide aqueous solution, followed byextraction with toluene. The collected organic layer was washed withsaturated brine and water, dried with anhydrous sodium sulfate,filtrated, concentrated, and vacuum-dried, thereby obtaining 77.50 g ofa crude product of an optically active secondary amine represented bythe following formula.

It was found by gas chromatography that conversion of the crude productwas 100% and that the ratio of a diastereomer of S—S configuration to adiastereomer of R—S configuration was 68:32.

The NMR data of the crude product are as follows.

¹H-NMR (TMS, CDCl₃) of S—S configuration, δppm: 0.72 (t, 7.4 Hz, 3H),1.25 (d, 6.4 Hz, 3H), 1.40-1.90 (m, 2H), 1.57 (br, 1H), 3.19 (t, 7.0 Hz,1H), 3.44 (q, 6.4 Hz, 1H), 6.92-7.36 (Ar—H, 9H).

¹H-NMR (TMS, CDCl₃) of R—S configuration, δppm: 0.75 (t, 7.4 Hz, 3H),1.33 (d, 6.4 Hz, 3H), 1.40-1.90 (m, 2H), 1.57 (br, 1H), 3.54 (dd, 5.2,8.4 Hz, 1H), 3.68 (q, 6.4 Hz, 1H), 6.92-7.36 (Ar—H, 9H).

Step (a), Alkylation

At first, 5.00 g (19.35 mmol, 1 eq.) of the above crude product of theoptically active secondary amine, 27.50 g (193.74 mmol, 10.01 eq.) ofmethyl iodide, and 5.36 g (38.78 mmol, 2.00 eq.) of anhydrous potassiumcarbonate were added to 19.4 ml of dimethylformamide, followed bystirring at 50° C. for 25 hr. After the reaction, the reaction liquidwas diluted with ethyl acetate, followed by washing with 1N sodiumhydroxide aqueous solution, drying with anhydrous sodium sulfate,filtration, concentration, and vacuum drying, thereby obtaining 5.46 gof a crude product of an optically active tertiary amine represented bythe following formula.

Conversion was found by gas chromatography to be 100%. Furthermore, thecrude product was purified by a silica gel column chromatography (ethylacetate : n-hexane=1:20), thereby obtaining 4.11 g of a purified productof the optically active tertiary amine. The total yield from thedehydration and condensation to the alkylation was 78%.

¹H-NMR (TMS, CDCl₃) of S—S configuration, δppm: 0.73 (t, 7.4 Hz, 3H),1.25 (d, 6.4 Hz, 3H), 1.56-2.06 (m, 2H), 2.09 (s, 3H), 3.47 (dd, 6.0,8.4 Hz, 1H), 3.64 (q, 6.4 Hz, 1H), 6.95-7.40 (Ar—H, 9H).

Step (b), Hydrogenolysis

To 3.7 ml of methanol, 1.00 g (3.69 mmol, 1 eq.) of the above purifiedproduct of the optically active tertiary amine, 1.11 g (18.48 mmol, 5.01eq.) of acetic acid, and 50.0 mg (0. 125 wt % in terms of Pd) of apalladium catalyst (having 5% palladium carried on an activated carboncontaining 50 wt % of water) were added. The hydrogen pressure wasadjusted to 0.5 MPa, and the stirring was conducted at 60° C. for 15 hr.After the reaction, the reaction liquid was filtrated using a filtrationaid (CELITE (trade name)), concentrated, and vacuum-dried, therebyobtaining a crude product of an acetate of an optically active(S)-1-(4-fluorophenyl)propylamine N-monomethyl, represented by thefollowing formula.

Then, 1N sodium hydroxide was added to the above crude product of theacetate to have a basic solution, followed by extraction with ethylacetate. The recovered organic layer was dried with anhydrous sodiumsulfate, followed by filtration, concentration, and vacuum drying,thereby obtaining 0.51 g of a crude product of an optically active(S)-1-(4-fluorophenyl)propylamine N-monomethyl represented by thefollowing formula.

The yield was 82%. The above crude product was found by chiral gaschromatography to have a conversion of 100% and an enantiomeric excessof 36% ee. In terms of severing position selectivity whether the N—C*bond is severed at the broken line “a” to produce a compound A or at thebroken line “b” to produce a compound B (i.e., the above opticallyactive (S)-1-(4-fluorophenyl)propylamine N-monomethyl) in the aboveformula 11, the above crude product was found by chiral gaschromatography to contain 1 part by mole of the compound A and 99 partsby mole of the compound B.

¹H-NMR (TMS, CDCl₃), δppm: 0.79 (t, 7.4 Hz, 3H), 1.61 (m, 1H), 1.66 (br,1H), 1.74 (m, 1H), 2.26 (s, 3H), 3.35 (dd, 5.6, 8.0 Hz, 1H), 7.00 (Ar—H,2H), 7.23 (Ar—H, 2H).

EXAMPLE 4 SYNTHESIS OF OPTICALLY ACTIVE(R)-1-(4-FLUOROPHENYL)PROPYLAMINE N-MONOMETHYL

Example 3 was repeated except in that (S)-1-phenylethylamine wasreplaced in the step (c) with (R)-1-phenylethylamine, thereby obtainingan optically active (R)-1-(4-fluorophenyl)propylamine N-monomethyl.

NMR data of an optically active tertiary amine, represented by thefollowing formula, are shown in the following.

¹H-NMR (TMS, CDCl₃) of R—R configuration, δppm: 0.73 (t, 7.4 Hz, 3H),1.25 (d, 6.4 Hz, 3H), 1.56-2.06 (m, 2H), 2.09 (s, 3H), 3.47 (dd, 6.0,8.4 Hz, 1H), 3.64 (q, 6.4 Hz, 1H), 6.95-7.40 (Ar—H, 9H).

NMR data of an optically active (R)-1-(4-fluorophenyl)propylamineN-monomethyl, represented by the following formula, are shown asfollows.

¹H-NMR (TMS, CDCl₃), δppm: 0.79 (t, 7.4 Hz, 3H), 1.61 (m, 1H), 1.66 (br,1H), 1.74 (m, 1H), 2.26 (s, 3H), 3.35 (dd, 5.6, 8.0 Hz, 1H), 7.00 (Ar—H,2H), 7.23 (Ar—H, 2H).

In chiral gas chromatography, the major enantiomer peaks of Example 4were identical with the minor enantiomer peaks of Example 3, and theminor enantiomer peaks of Example 4 were identical with the majorenantiomer peaks of Example 3.

EXAMPLE 5 SYNTHESIS OF OPTICALLY ACTIVE(S)-1-(4-TRIFLUOROMETHYLPHENYL)ETHYLAMINE N-MONOMETHYL Step (c),Dehydration and Condensation

At first, 5.02 g (26.68 mmol, 1 eq.) of 4-trifluoromethylphenyl methylketone, 3.67 g (30.29 mmol, 1.14 eq.) of (S)-1-phenylethylamine, and0.11 g (0.81 mmol, 0.03 eq.) of zinc chloride were added to 27 ml oftoluene. The resulting mixture was stirred for 15 hr under a heatedreflux condition, while water (by-product) was removed from a Dean-Starktrap. The resulting reaction liquid was washed with 5% sodium hydroxideaqueous solution, 1.5N ammonium chloride aqueous solution, and water.The recovered organic layer was dried with anhydrous sodium sulfate,filtrated, concentrated and vacuum-dried, thereby obtaining 8.20 g of acrude product of an optically active imine represented by the followingformula.

Conversion was found by gas chromatography to be 99%.

¹H-NMR (TMS; CDCl₃), δppm: 1.54 (d, 6.6 Hz, 3H), 2.29 (s, 3H), 4.85 (q,6.6 Hz, 1H), 7.24 (Ar—H, 1H), 7.34 (Ar—H, 2H), 7.46 (Ar—H, 2H), 7.63(Ar—H, 2H), 7.94 (Ar—H, 2H).

Step (d), Asymmetric Reduction

At first, 8.20 g (26.68 mmol, 1 eq.) of the crude product of theoptically active imine produced by the above step (c) were added to 22ml of methanol. The resulting solution was cooled down to 0° C. Then,1.06 g (28.02 mmol, 1.05 eq.) of sodium borohydride were added, followedby stirring for 5.5 hr at the same temperature. After the reaction, 1Nhydrochloric acid aqueous solution was added to decompose the remainingsodium borohydride. Then, the reaction liquid was made basic by adding1N sodium hydroxide aqueous solution, followed by extraction withtoluene. The collected organic layer was washed with water, dried withanhydrous sodium sulfate, filtrated, concentrated, and vacuum-dried,thereby obtaining 7.91 g of a crude product of an optically activesecondary amine represented by the following formula.

It was found by gas chromatography that conversion of the crude productwas 100% and that the ratio of a diastereomer of S—S configuration to adiastereomer of R—S configuration was 84:16.

¹H-NMR (TMS, CDCl₃) of S—S configuration, δppm: 1.27 (d, 6.6 Hz, 3H),1.29 (d, 6.6 Hz, 3H), 1.59 (br, 1H), 3.45 (q, 6.6 Hz, 1H), 3.57 (q, 6.6Hz, 1H), 7.12-7.67 (Ar—H, 9H).

¹H-NMR (TMS, CDCl₃) of R—S configuration, δppm: 1.37 (d, 6.8 Hz, 6H),1.59 (br, 1H), 3.76 (q, 6.8 Hz, 1H), 3.84 (q, 6.8 Hz, 1H), 7.12-7.67(Ar—H, 9H)

Steps (e) and (f), Salt Formation and its Recrystallization

3.00 g (10.12 mmol, 1 eq.) of the crude product of the optically activesecondary amine produced by the above step (d) and 1.68 g (10.11 mmol,1.00 eq.) of phthalic acid were added to 10.5 ml of i-propanol, followedby stirring at 70° C. for 40 min. Then, 15 ml of n-hexane were added,followed by allowing it to cool down to room temperature and thenallowing it to stand still for 12 hr. The precipitated crystals werefiltered, washed with a small amount of n-hexane, and vacuum-dried,thereby obtaining 3.74 g of crystals of a phthalate of the opticallyactive secondary amine, which is represented by the following formula.

The diastereomeric excess of the crystals was determined by gaschromatography in a manner that the phthalate was turned into a freebase with 0.5N sodium hydroxide aqueous solution. The result was 94.2%de. Furthermore, 3.60 g of the above crystals of the phthalate wereadded to 9 ml of i-propanol, followed by stirring at 70° C. for 40 min,adding 6 ml of n-hexane, allowing it to cool down to room temperature,and allowing it to stand still for 12 hr. The precipitated crystals werefiltrated, followed by washing with a small amount of n-hexane andvacuum drying, thereby obtaining 3.30 g of crystals of the abovephthalate of the optically active secondary amine. The diastereomericexcess of the crystals was determined by gas chromatography in a mannerthat the phthalate was turned into a free base with 0.5N sodiumhydroxide aqueous solution. The result was 99.1% de. The total yieldfrom the dehydration and the condensation to the salt formation and itsrecrystallization was 74%.

¹H-NMR (TMS, CDCl₃), δppm: 1.80 (d, 6.8 Hz, 6H), 4.04 (q, 6.8 Hz, 1H),4.13 (q, 6.8 Hz, 1H), 7.35-7.73 (Ar—H, 11H), 8.45-8.55 (Ar—H, 2H), 10.60(br, 3H).

Then, 0.5N sodium hydroxide aqueous solution was added to 3.00 g (6.53mmol) of the crystals of the phthalate to have a basic solution,followed by extraction with toluene. The collected organic layer waswashed with saturated brine, dried with anhydrous sodium sulfate,filtrated, concentrated, and vacuum-dried, thereby obtaining 1.92 g of apurified product of an optically active secondary amine represented bythe following formula.

The recovery was quantitative.

¹H-NMR (TMS, CDCl₃), δppm: 1.27 (d, 6.6 Hz, 3H), 1.29 (d, 6.6 Hz, 3H),1.59 (br, 1H), 3.45 (q, 6.6 Hz, 1H), 3.57 (q, 6.6 Hz, 1H), 7.12-7.67(Ar—H, 9H).

Step (a), Alkylation

At first, 0.80 g (2.73 mmol, 1 eq.) of the above purified product of theoptically active secondary amine, 3.88 g (27.34 mmol, 10.01 eq.) ofmethyl iodide, and 0.75 g (5.43 mmol, 1.99 eq.) of anhydrous potassiumcarbonate were added to 2.7 ml of dimethylformamide, followed bystirring at room temperature for 17 hr. After the reaction, the reactionliquid was diluted with a mixed solution of ethyl acetate and n-hexane(ethyl acetate : n-hexane=1:10), followed by washing with water, 1Nsodium hydroxide aqueous solution and saturated brine, drying withanhydrous sodium sulfate, filtration, concentration, and vacuum drying,thereby obtaining 0.98 g of a crude product of an optically activetertiary amine represented by the following formula.

Conversion was found by gas chromatography to be 98%. Furthermore, thecrude product was purified by a silica gel column chromatography(n-hexane), thereby obtaining 0.62 g of a purified product of theoptically active tertiary amine. The yield was 74%.

¹H-NMR (TMS, CDCl₃), δppm: 1.33 (d, 6.8 Hz, 3H), 1.35 (d, 6.8 Hz, 3H),1.98 (s, 3H), 3.81 (q, 6.8 Hz, 1H), 3.88 (q, 6.8 Hz, 1H), 7.20-7.63(Ar—H, 9H).

Step (b), Hydrogenolysis

To 1.6 ml of methanol, 0.50 g (1.63 mmol, 1 eq.) of the above purifiedproduct of the optically active tertiary amine, 0.49 g (8.16 mmol, 5.01eq.) of acetic acid, and 24.9 mg (0.125 wt % Pd) of a palladium catalyst(having 5% palladium carried on an activated carbon containing 50 wt %of water) were added. The hydrogen pressure was adjusted to 0.5 MPa, andthe stirring was conducted at 60° C. for 13.5 hr. After the reaction,the reaction liquid was filtrated using a filtration aid (CELITE (tradename)), concentrated, and vacuum-dried, thereby obtaining a crudeproduct of an acetate of an optically active(S)-1-(4-trifluoromethylphenyl)ethylamine N-monomethyl, represented bythe following formula.

Then, 1N sodium hydroxide aqueous solution was added to the above crudeproduct of the acetate to have a basic solution, followed by extractionwith ethyl acetate. The recovered organic layer was dried with anhydroussodium sulfate, followed by filtration, concentration, and vacuumdrying, thereby obtaining 0.31 g of a crude product of an opticallyactive (S)-1-(4-trifluoromethylphenyl)ethylamine N-monomethylrepresented by the following formula.

The yield was 94%. The above crude product was found by chiral gaschromatography to have a conversion of 100% and an enantiomeric excessof 99.1% ee. In terms of severing position selectivity whether the N—C*bond is severed at the broken line “a” to produce a compound A or at thebroken line “b” to produce a compound B (i.e., the above opticallyactive (S)-1-(4-trifluoromethylphenyl)ethylamine N-monomethyl) in theabove formula 11, the above crude product was found by chiral gaschromatography to contain 1 part by mole of the compound A and 100 partsby mole of the compound B.

¹H-NMR (TMS, CDCl₃), δppm: 1.51 (d, 6.8 Hz, 3H), 2.35 (s, 3H), 3.88 (q,6.8 Hz, 1H), 5.16 (br, 1H), 7.54 (Ar—H, 2H), 7.63 (Ar—H, 2H).

EXAMPLE 6 SYNTHESIS OF OPTICALLY ACTIVE(R)-1-(4-TRIFLUOROMETHYLPHENYL)ETHYLAMINE N-MONOMETHYL

Example 5 was repeated except in that (S)-1-phenylethylamine wasreplaced in the step (c) with (R)-1-phenylethylamine, thereby obtainingan optically active (R)-1-(4-trifluoromethylphenyl)ethylamineN-monomethyl.

NMR data of an optically active tertiary amine, represented by thefollowing formula, are shown as follows.

¹H-NMR (TMS, CDCl₃), δppm: 1.33 (d, 6.8 Hz, 3H), 1.35 (d, 6.8 Hz, 3H),1.98 (s, 3H), 3.81 (q, 6.8 Hz, 1H), 3.88 (q, 6.8 Hz, 1H), 7.20-7.63(Ar—H, 9H).

NMR data of an optically active(R)-1-(4-trifluoromethylphenyl)ethylamine N-monomethyl, represented bythe following formula, are shown as follows.

¹H-NMR (TMS, CDCl₃), δppm: 1.51 (d, 6.8 Hz, 3H), 2.35 (s, 3H), 3.88 (q,6.8 Hz, 1H), 5.16 (br, 1H), 7.54 (Ar—H, 2H), 7.63 (Ar—H, 2H).

In chiral gas chromatography, the major enantiomer peaks of Example 6were identical with the minor enantiomer peaks of Example 5, and theminor enantiomer peaks of Example 6 were identical with the majorenantiomer peaks of Example 5.

EXAMPLE 7 SYNTHESIS OF OPTICALLY ACTIVE(S)-1-(4-TRIFLUOROMETHYLPHENYL)ETHYLAMINE N-MONOETHYL Step (a),Alkylation

At first, (a) 0.80 g (2.73 mmol, 1 eq.) of the purified product of theoptically active secondary amine, produced by the “salt formation andits recrystallization” of Example 5, (b) 8.51 g (54.56 mmol, 19.99 eq.)of ethyl iodide, and (c) 0.75 g (5.43 mmol, 1.99 eq.) of anhydrouspotassium carbonate were added to 2.7 ml of dimethylformamide, followedby stirring at 100° C. for 21 hr. After the reaction, the reactionliquid was diluted with ethyl acetate, followed by washing with 1Nsodium hydroxide aqueous solution and saturated brine, drying withanhydrous sodium sulfate, filtration, concentration, and vacuum drying,thereby obtaining 0.82 g of a crude product of an optically activetertiary amine represented by the following formula.

Conversion was found by gas chromatography to be 99%. Furthermore, thecrude product was purified by a silica gel column chromatography (ethylacetate: n-hexane=1:20), thereby obtaining 0.77 g of a purified productof the optically active tertiary amine. The yield was 88%.

¹H-NMR (TMS, CDCl₃), δppm: 0.83 (t, 7.0 Hz, 3H), 1.39 (d, 6.8 Hz, 3H),1.40 (d, 6.8 Hz, 3H), 2.49 (m, 1H), 2.68 (m, 1H), 4.02 (m, 2H),7.17-7.57 (Ar—H, 9H).

Step (b), Hydrogenolysis

To 2.2 ml of methanol, 0.70 g (2.18 mmol, 1 eq.) of the above purifiedproduct of the optically active tertiary amine, 0.65 g (10.82 mmol, 4.96eq.) of acetic acid, and 35.0 mg (0.125 wt % Pd) of a palladium catalyst(having 5% palladium carried on an activated carbon containing 50 wt %of water) were added. The hydrogen pressure was adjusted to 0.5 MPa, andthe stirring was conducted at 60° C. for 17 hr. After the reaction, thereaction liquid was filtrated using a filtration aid (CELITE (tradename)), concentrated, and vacuum-dried, thereby obtaining a crudeproduct of an acetate of an optically active(S)-1-(4-trifluoromethylphenyl)ethylamine N-monoethyl, represented bythe following formula.

Then, 1N sodium hydroxide aqueous solution was added to the above crudeproduct of the acetate to have a basic solution, followed by extractionwith ethyl acetate. The recovered organic layer was dried with anhydroussodium sulfate, followed by filtration, concentration, and vacuumdrying, thereby obtaining 0.42 g of a crude product of an opticallyactive (S)-1-(4-trifluoromethylphenyl)ethylamine N-monoethyl representedby the following formula.

The yield was 89%. The above crude product was found by chiral gaschromatography to have a conversion of 100% and an enantiomeric excessof 99.1% ee. In terms of severing position selectivity whether the N—C*bond is severed at the broken line “a” to produce a compound A or at thebroken line “b” to produce a compound B (i.e., the above opticallyactive (S)-1-(4-trifluoromethylphenyl)ethylamine N-monoethyl) in theabove formula 11, the above crude product was found by chiral gaschromatography to contain 1 part by mole of the compound A and 99 partsby mole of the compound B.

¹H-NMR (TMS, CDCl₃), δppm: 1.08 (t, 7.2 Hz, 3H), 1.35 (d, 6.8 Hz, 3H),1.35 (br, 1H), 2.38-2.60 (m, 2H), 3.85 (q, 6.8 Hz, 1H), 7.44 (Ar—H, 2H),7.58 (Ar—H, 2H).

EXAMPLE 8 SYNTHESIS OF OPTICALLY ACTIVE(R)-1-(4-TRIFLUOROMETHYLPHENYL)ETHYLAMINE N-MONOETHYL

Example 7 was repeated except in that the purified product of theoptically active secondary amine, produced by the “salt formation andits recrystallization” of Example 5, was replaced with that of Example6, thereby obtaining an optically active(R)-1-(4-trifluoromethylphenyl)ethylamine N-monoethyl.

NMR data of an optically active tertiary amine, represented by thefollowing formula, are shown as follows.

¹H-NMR (TMS, CDCl₃), δppm: 0.83 (t, 7.0 Hz, 3H), 1.39 (d, 6.8 Hz, 3H),1.40 (d, 6.8 Hz, 3H), 2.49 (m, 1H), 2.68 (m, 1H), 4.02 (m, 2H),7.17-7.57 (Ar—H, 9H).

NMR data of an optically active(R)-1-(4-trifluoromethylphenyl)ethylamine N-monoethyl, represented bythe following formula, are shown as follows.

¹H-NMR (TMS, CDCl₃), δppm: 1.08 (t, 7.2 Hz, 3H), 1.35 (d, 6.8 Hz, 3H),1.35 (br, 1H), 2.38-2.60 (m, 2H), 3.85 (q, 6.8Hz, 1H), 7.44 (Ar—H, 2H),7.58 (Ar—H, 2H).

EXAMPLE 9 SYNTHESIS OF OPTICALLY ACTIVE(S)-1-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)ETHYLAMINE N-MONOMETHYL Step (c),Dehydration and Condensation

At first, 10.00 g (39.04 mmol, 1 eq.) of 3,5-bis(trifluoromethyl)phenylmethyl ketone, 4.96 g (40.93 mmol, 1.05 eq.) of (S)-1-phenylethylamine,and 0.37 g (1.95 mmol, 0.05 eq.) of p-toluenesulfonic acid monohydratewere added to 100 ml of toluene. The resulting mixture was stirred for24 hr under a heated reflux condition, while water (by-product) wasremoved from a Dean-Stark trap. The resulting reaction liquid was washedwith a saturated sodium hydrogencarbonate aqueous solution. Therecovered organic layer was dried with anhydrous magnesium sulfate,filtrated, concentrated and vacuum-dried, thereby obtaining 14.34 g of acrude product of an optically active imine represented by the followingformula.

The yield was quantitative.

¹H-NMR (TMS; CDCl₃), δppm: 1.55 (d, 6.4 Hz, 3H), 2.33 (s, 3H), 4.87 (q,6.4 Hz, 1H), 7.24 (Ar—H, 1H), 7.35 (Ar—H, 2H), 7.45 (Ar—H, 2H), 8.31(Ar—H, 1H), 8.38 (Ar—H, 2H).

Step (d), Asymmetric Reduction

At first, 14.34 g (39.04 mmol, 1 eq.) of the crude product of theoptically active imine produced by the above step (c) were added to 156ml of methanol. The resulting solution was cooled down to 0° C. Then,1.48 g (39.12 mmol, 1.00 eq.) of sodium borohydride were added, followedby stirring for 5 hr at the same temperature. After the reaction, 1Nhydrochloric acid aqueous solution was added to decompose the remainingsodium borohydride. Then, the reaction liquid was made basic by adding1N sodium hydroxide aqueous solution, followed by extraction withtoluene. The collected organic layer was washed with water, dried withanhydrous sodium sulfate, filtrated, concentrated, and vacuum-dried,thereby obtaining 14.31 g of a crude product of an optically activesecondary amine represented by the following formula.

It was found by gas chromatography that conversion of the crude productwas 100% and that the ratio of a diastereomer of S—S configuration to adiastereomer of R—S configuration was 84:16.

¹H-NMR (TMS, CDCl₃) of S—S configuration, δppm: 1.28 (d, 6.5 Hz, 3H),1.29 (d, 6.4 Hz, 3H), 1.58 (br, 1H), 3.39 (q, 6.5 Hz, 1H), 3.65 (q, 6.4Hz, 1H), 7.05-7.44 (Ar—H, 5H), 7.70 (Ar—H, 2H), 7.76 (Ar—H, 1H).

¹H-NMR (TMS, CDCl₃) of R—S configuration, δppm: 1.37 (d, 6.5 Hz, 3H),1.38 (d, 6.5 Hz, 3H), 1.52 (br, 1H), 3.78 (q, 6.5 Hz, 1H), 3.87 (q, 6.5Hz, 1H), 7.10-7.33 (Ar—H, 5H), 7.65 (Ar—H, 1H), 7.67 (Ar—H, 2H).

Steps (e) and (f), Salt Formation and its Recrystallization

14.31 g (39.04 mmol, 1 eq.) of the crude product of the optically activesecondary amine produced by the above step (d) and 7.43 g (39.06 mmol,1.00 eq.) of p-toluenesulfonic acid monohydrate were added to 23.4 ml ofi-propanol, followed by stirring at 60° C. for 40 min. Then, 28.1 ml ofn-heptane were added, followed by allowing it to cool down to roomtemperature and then stirring for 12 hr. The precipitated crystals werefiltered, washed with a small amount of n-heptane, and vacuum-dried,thereby obtaining 10.90 g of crystals of a p-toluenesulfonate of theoptically active secondary amine, which is represented by the followingformula.

The diastereomeric excess of the crystals was determined by gaschromatography in a manner that the p-toluenesulfonate was turned into afree base with 1N sodium hydroxide aqueous solution. The result was99.7% de. The total yield from the dehydration and the condensation tothe salt formation and its recrystallization was 52%.

¹H-NMR (TMS, DMSO-d₆), δppm: 1.55 (d, 6.0 Hz, 3H), 1.58 (d, 6.0 Hz, 3H),2.28 (s, 3H), 4.29 (q, 6.0 Hz, 1H), 4.54 (q, 6.0 Hz, 1H), 7.11 (Ar—H,2H), 7.38 (Ar—H, 2H), 7.43 (Ar—H, 3H), 7.47 (Ar—H, 2H), 8.10 (Ar—H, 2H),8.20 (Ar—H, 1H), 9.41 (br, 2H).

Then, 1N sodium hydroxide aqueous solution was added to 8.00 g (14.99mmol) of the crystals of the p-toluenesulfonate to have a basicsolution, followed by extraction with toluene. The collected organiclayer was washed with saturated brine, dried with anhydrous sodiumsulfate, filtrated, concentrated, and vacuum-dried, thereby obtaining5.42 g of a purified product of an optically active secondary aminerepresented by the following formula.

The recovery was quantitative.

¹H-NMR (TMS, CDCl₃), δppm: 1.28 (d, 6.5 Hz, 3H), 1.29 (d, 6.4 Hz, 3H),1.58 (br, 1H), 3.39 (q, 6.5 Hz, 1H), 3.65 (q, 6.4 Hz, 1H), 7.05-7.44(Ar—H, 5H), 7.70 (Ar—H, 2H), 7.76 (Ar—H, 1H).

Step (a), Alkylation

At first, 3.78 g (10.46 mmol, 1 eq.) of the above purified product ofthe optically active secondary amine, 2.96 g (20.85 mmol, 1.99 eq.) ofmethyl iodide, and 2.89 g (20.91 mmol, 2.00 eq.) of anhydrous potassiumcarbonate were added to a mixed solution of 2.6 ml of dimethylformamideand 7.8 ml of tetrahydrofuran, followed by stirring at 58° C. for 43 hr.After the reaction, the reaction liquid was diluted with ethyl acetate,followed by washing with saturated brine, drying with anhydrous sodiumsulfate, filtration, concentration, and vacuum drying, thereby obtaining5.72 g of a crude product of an optically active tertiary aminerepresented by the following formula.

Conversion was found by gas chromatography to be 94%. Furthermore, thecrude product was purified by a silica gel column chromatography (ethylacetate : n-hexane=1:10), thereby obtaining 3.50 g of a purified productof the optically active tertiary amine. The yield was 89%.

¹H-NMR (TMS, CDCl₃), δppm: 1.37 (d, 6.8 Hz, 3H), 1.38 (d, 6.8 Hz, 3H),2.00 (s, 3H), 3.76 (q, 6.8 Hz, 1H), 4.00 (q, 6.8 Hz, 1H), 7.20-7.40(Ar—H, 5H), 7.76 (Ar—H, 1H), 7.82 (Ar—H, 2H).

Step (b), Hydrogenolysis

To 8.0 ml of methanol, 3.00 g (7.99 mmol, 1 eq.) of the above purifiedproduct of the optically active tertiary amine and 60.0 mg (0.05 wt %Pd) of a palladium catalyst (having 5% palladium carried on an activatedcarbon containing 50 wt % of water) were added. The hydrogen pressurewas adjusted to 0.5 MPa, and the stirring was conducted at 60° C. for 21hr. After the reaction, the reaction liquid was filtrated using afiltration aid (CELITE (trade name)), concentrated, and vacuum-dried,thereby obtaining 2.04 g of a crude product of an optically active(S)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monomethyl,represented by the following formula.

The above crude product was found by chiral gas chromatography to have aconversion of 97% and an enantiomeric excess of 99.7% ee. In terms ofsevering position selectivity whether the N—C* bond is severed at thebroken line “a” to produce a compound A or at the broken line “b” toproduce a compound B (i.e., the above optically active(S)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monomethyl) in theabove formula 11, the above crude product was found by chiral gaschromatography to contain 1 part by mole of the compound A and 99 partsby mole of the compound B. Furthermore, the above crude product waspurified by a distillation, thereby obtaining 1.58 g of a purifiedproduct of the optically active(S)-1-(3,5-(bis(trifluoromethyl)phenyl)ethylamine N-monomethyl. Theyield was 73%.Boiling Point: 90-95° C./1070 Pa.[α]²⁵ _(D): -34.7.

¹H-NMR (TMS, CDCl₃), δppm: 1.38 (d, 6.4 Hz, 3H), 1.45 (br, 1H), 2.30 (s,3H), 3.81 (q, 6.4 Hz, 1H), 7.75 (Ar—H, 1H), 7.80 (Ar—H, 2H).

EXAMPLE 10 SYNTHESIS OF OPTICALLY ACTIVE(R)-1-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)ETHYLAMINE N-MONOMETHYL

Example 9 was repeated except in that (S)-1-phenylethylamine wasreplaced in the step (c) with (R)-1-phenylethylamine, thereby obtainingan optically active (R)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamineN-monomethyl.

NMR data of an optically active tertiary amine, represented by thefollowing formula, are shown as follows.

¹H-NMR (TMS, CDCl₃), δppm: 1.37 (d, 6.8 Hz, 3H), 1.38 (d, 6.8 Hz, 3H),2.00 (s, 3H), 3.76 (q, 6.8 Hz, 1H), 4.00 (q, 6.8 Hz, 1H), 7.20-7.40(Ar—H, 5H), 7.76 (Ar—H, 1H), 7.82 (Ar—H, 2I[).

NMR data of an optically active(R)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monomethyl,represented by the following formula, are shown as follows.

¹H-NMR (TMS, CDCl₃), δppm: 1.38 (d, 6.4 Hz, 3H), 1.45 (br, 1H), 2.30 (s,3H), 3.81 (q, 6.4 Hz, 1H), 7.75 (Ar—H, 1H), 7.80 (Ar—H, 2H).

In chiral gas chromatography, the major enantiomer peaks of Example 10were identical with the minor enantiomer peaks of Example 9, and theminor enantiomer peaks of Example 10 were identical with the majorenantiomer peaks of Example 9.

EXAMPLE 11 SYNTHESIS OF OPTICALLY ACTIVE(R)-1-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)ETHYLAMINE N-MONOMETHYL Steps (e)and (f), Salt Formation and its Recrystallization

The mother liquor obtained by the “salt formation and itsrecrystallization” of Example 9 was concentrated, followed by adding 1Nsodium hydroxide aqueous solution to have basicity and then extractionwith toluene. The collected organic layer was washed with saturatedbrine, followed by drying with anhydrous sodium sulfate, filtration,concentration and vacuum drying, thereby obtaining 6.97 g of anoptically active secondary amine (recovered from the above motherliquor) represented by the following formula.

The recovery was quantitative. It was found by gas chromatography thatthat the ratio of a diastereomer of S—S configuration to a diastereomerof R—S configuration of the secondary amine was 67:33. The total amountof 6.97 g (18.61 mmol, 1 eq.) of the secondary amine and 1.08 g (9.30mmol, 0.50 eq.) of fumaric acid were added to a mixed solution of 2.2 mlof i-propanol and 22.3 ml of n-heptane, followed by stirring at 80° C.for 2 hr, then allowing it to cool down to room temperature, and thenstirring for 12 hr at room temperature. The precipitated crystals werefiltered, washed with a small amount of n-heptane, and vacuum-dried,thereby obtaining 2.02 g of crystals of a fumarate of the opticallyactive secondary amine, which is represented by the following formula.

The diastereomeric excess of the crystals was determined by gaschromatography in a manner that the fumarate was turned into a free basewith 1N sodium hydroxide aqueous solution. The result was 98.5% de.Furthermore, 2.00 g of the above fumarate were added to 7.3 ml ofi-propanol, followed by dissolution at 80° C., allowing it to cool downto room temperature and stirring for 12 hr. The precipitated crystalswere filtered, washed with a small amount of n-heptane, andvacuum-dried, thereby obtaining 1.72 g of crystals of a fumarate of theoptically active secondary amine, which is represented by the aboveformula. The diastereomeric excess of the crystals was determined by gaschromatography in a manner that the fumarate was turned into a free basewith 1N sodium hydroxide aqueous solution. The result was 100% de. Therecovery of the fumarate of the optically active secondary amine (R—Sconfiguration) from the mother liquor obtained by the “salt formationand its recrystallization of Example 9” was 59%.

¹H-NMR (standard substance: TMS; solvent: DMSO-d₆), δppm: 1.26 (d, 6.6Hz, 3H), 1.29 (d, 6.6 Hz, 3H), 3.49 (br, 3H), 3.67 (q, 6.6 Hz, 1H), 3.93(q, 6.6 Hz, 1H), 6.60 (s, 2H), 7.00-7.25 (Ar—H, 5H), 7.81 (Ar—H, 1H),7.93 (Ar—H, 2H).

Then, 1N sodium hydroxide aqueous solution was added to 1.70 g (3.56mmol) of the crystals (100% de) of the fumarate to have a basicsolution, followed by extraction with toluene. The collected organiclayer was washed with saturated brine, dried with anhydrous sodiumsulfate, filtrated, concentrated, and vacuum-dried, thereby obtaining1.29 g of a purified product of an optically active secondary aminerepresented by the following formula.

The recovery was quantitative.

¹H-NMR (TMS, CDCl₃), δppm: 1.37 (d, 6.5 Hz, 3H), 1.38 (d, 6.5 Hz, 3H),1.52 (br, 1H), 3.78 (q, 6.5 Hz, 1H), 3.87 (q, 6.5 Hz, 1H), 7.10-7.33(Ar—H, 5H), 7.65 (Ar—H, 1H), 7.67 (Ar—H, 2H).

Step (a), Alkylation

At first, 1.08 g (2.99 mmol, 1 eq.) of the above purified product (100%de) of the optically active secondary amine, 4.33 g (30.51 mmol, 10.20eq.) of methyl iodide, and 0.83 g (6.01 mmol, 2.01 eq.) of anhydrouspotassium carbonate were added to 3.0 ml of dimethylformamide, followedby stirring at room temperature for 18 hr. After the reaction, thereaction liquid was diluted with ethyl acetate, followed by washing withwater and saturated brine, drying with anhydrous sodium sulfate,filtration, concentration, and vacuum drying, thereby obtaining 1.11 gof a crude product of an optically active tertiary amine represented bythe following formula.

Conversion was found by gas chromatography to be 100%. Furthermore, thecrude product was purified by a silica gel column chromatography (ethylacetate : n-hexane=5:95), thereby obtaining 0.97 g of a purified productof the optically active tertiary amine. The yield was 87%.

¹H-NMR (TMS, CDCl₃), δppm: 1.33 (d, 6.8 Hz, 3H), 1.37 (d, 6.8 Hz, 3H),2.12 (s, 3H), 3.73 (q, 6.8 Hz, 1H), 3.86 (q, 6.8 Hz, 1H), 7.20-7.43(Ar—H, 5H), 7.72 (Ar—H, 1H), 7.87 (Ar—H, 2H).

Step (b), Hydrogenolysis

To 2.4 ml of methanol, 0.90 g (2.40 mmol, 1 eq.) of the above purifiedproduct of the optically active tertiary amine and 18.0 mg (0.05 wt %Pd) of a palladium catalyst (having 5% palladium carried on an activatedcarbon containing 50 wt % of water) were added. The hydrogen pressurewas adjusted to 0.5 MPa, and the stirring was conducted at 60° C. for17.5 hr. After the reaction, the reaction liquid was filtrated using afiltration aid (CELITE (trade name)), concentrated, and vacuum-dried,thereby obtaining 0.60 g of a crude product of an optically active(R)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monomethyl,represented by the following formula.

The yield was 92%. The above crude product was found by chiral gaschromatography to have a conversion of 100% and an enantiomeric excessof 100% ee. In terms of severing position selectivity whether the N—C*bond is severed at the broken line “a” to produce a compound A or at thebroken line “b” to produce a compound B (i.e., the above opticallyactive (R)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monomethyl) inthe above formula 11, the above crude product was found by chiral gaschromatography to contain 1 part by mole of the compound A and 99 partsby mole of the compound B.

¹H-NMR (TMS, CDCl₃), δppm: 1.38 (d, 6.4 Hz, 3H), 1.45 (br, 1H), 2.30 (s,3H), 3.81 (q, 6.4 Hz, 1H), 7.75 (Ar—H, 1H), 7.80 (Ar—H, 2H).

EXAMPLE 12 SYNTHESIS OF OPTICALLY ACTIVE(S)-1-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)ETHYLAMINE N-MONOMETHYL

Example 11 was repeated except in that the mother liquor obtained by the“salt formation and its recrystallization” of Example 9 was replacedwith that of Example 10, thereby obtaining an optically active(S)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monomethyl.

NMR data of an optically active tertiary amine, represented by thefollowing formula, are shown as follows.

¹H-NMR (TMS, CDCl₃), δppm: 1.33 (d, 6.8 Hz, 3H), 1.37 (d, 6.8 Hz, 3H),2.12 (s, 3H), 3.73 (q, 6.8 Hz, 1H), 3.86 (q, 6.8 Hz, 1H), 7.20-7.43(Ar—H, 5H), 7.72 (Ar—H, 1H), 7.87 (Ar—H, 2H).

NMR data of an optically active(S)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monomethyl,represented by the following formula, are shown as follows.

¹H-NMR (TMS, CDCl₃), δppm: 1.38 (d, 6.4 Hz, 3H), 1.45 (br, 1H), 2.30 (s,3H), 3.81 (q, 6.4 Hz, 1H), 7.75 (Ar—H, 1H), 7.80 (Ar—H, 2H).

In chiral gas chromatography, the major enantiomer peaks of Example 12were identical with the minor enantiomer peaks of Example 11, and theminor enantiomer peaks of Example 12 were identical with the majorenantiomer peaks of Example 11.

EXAMPLE 13 SYNTHESIS OF OPTICALLY ACTIVE(S)-1-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)ETHYLAMINE N-MONOETHYL Step (a),Alkylation

At first, 1.50 g (4.15 mmol, 1 eq.) of the purified product of theoptically active secondary amine produced by the “salt formation and itsrecrystallization” of Example 9, 9.71 g (62.26 mmol, 15.00 eq.) of ethyliodide, and 1.15 g (8.32 mmol, 2.00 eq.) of anhydrous potassiumcarbonate were added to 4.2 ml of dimethylformamide, followed bystirring at 100° C. for 21 hr. After the reaction, the reaction liquidwas diluted with a mixed solution of 1 part by volume of ethyl acetateand 1 part by volume of n-hexane, followed by washing with saturatedbrine, drying with anhydrous sodium sulfate, filtration, concentration,and vacuum drying, thereby obtaining 2.12 g of a crude product of anoptically active tertiary amine represented by the following formula.

Conversion was found by gas chromatography to be 92%. Furthermore, thecrude product was purified by a silica gel column chromatography(n-hexane), thereby obtaining 1.32 g of a purified product of theoptically active tertiary amine. The yield was 81%.

¹H-NMR (TMS, CDCl₃), δppm: 0.89 (t, 7.2 Hz, 3H), 1.43 (d, 6.8 Hz, 3H),1.45 (d, 6.8 Hz, 3H), 2.51 (m, 1H), 2.70 (m, 1H), 4.02 (q, 6.8 Hz, 1H),4.08 (q, 6.8 Hz, 1H), 7.15-7.43 (Ar—H, 5H), 7.68 (Ar—H, 1H), 7.77 (Ar—H,2H).

Step (b), Hydrogenolysis

To 1.7 ml of methanol, 0.66 g (1.70 mmol, 1 eq.) of the above purifiedproduct of the optically active tertiary amine, 0.83 g (13.82 mmol, 8.13eq.) of acetic acid, and 53.3 mg (0.202 wt % Pd) of a palladium catalyst(having 5% palladium carried on an activated carbon containing 50 wt %of water) were added. The hydrogen pressure was adjusted to 0.5-0.6 MPa,and the stirring was conducted at 60-70° C. for 36 hr. After thereaction, the reaction liquid was filtrated using a filtration aid(CELITE (trade name)), concentrated, and vacuum-dried, thereby obtaining0.43 g of a crude product of an optically active(S)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monoethyl,represented by the following formula.

The yield was 90%. The above crude product was found by chiral gaschromatography to have a conversion of 100% and an enantiomeric excessof 99.7% ee. In terms of severing position selectivity whether the N—C*bond is severed at the broken line “a” to produce a compound A or at thebroken line “b” to produce a compound B (i.e., the above opticallyactive (S)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monoethyl) inthe above formula 11, the above crude product was found by chiral gaschromatography to contain 1 part by mole of the compound A and 99 partsby mole of the compound B.

¹H-NMR (TMS, CDCl₃), δppm: 1.09 (t, 7.2 Hz, 3H), 1.37 (d, 6.4 Hz, 3H),1.40 (br, 1H), 2.36-2.49 (m, 1H), 2.49-2.63 (m, 1H), 3.92 (q, 6.4 Hz,1H), 7.75 (Ar—H, 1H), 7.81 (Ar—H, 2H).

EXAMPLE 14 SYNTHESIS OF OPTICALLY ACTIVE(R)-1-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)ETHYLAMINE N-MONOETHYL

Example 13 was repeated except in that the purified product of theoptically active secondary amine produced by the “salt formation and itsrecrystallization” of Example 9 was replaced in the step (a) with thatof Example 10, thereby obtaining an optically active(R)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monoethyl.

NMR data of an optically active tertiary amine, represented by thefollowing formula, are shown as follows.

¹H-NMR (TMS, CDCl₃), δppm: 0.89 (t, 7.2 Hz, 3H), 1.43 (d, 6.8 Hz, 3H),1.45 (d, 6.8 Hz, 3H), 2.51 (m, 1H), 2.70 (m, 1H), 4.02 (q, 6.8 Hz, 1H),4.08 (q, 6.8 Hz, 1H), 7.15-7.43 (Ar—H, 5H), 7.68 (Ar—H, 1H), 7.77 (Ar—H,2H).

NMR data of an optically active(R)-1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monoethyl,represented by the following formula, are shown as follows.

¹H-NMR (TMS, CDCl₃), δppm: 1.09 (t, 7.2 Hz, 3H), 1.37 (d, 6.4 Hz, 3H),1.40 (br, 1H), 2.36-2.49 (m, 1H), 2.49-2.63 (m, 1H), 3.92 (q, 6.4 Hz,1H), 7.75 (Ar—H, 1H), 7.81 (Ar—H, 2H).

In chiral gas chromatography, the major enantiomer peaks of Example 14were identical with the minor enantiomer peaks of Example 13, and theminor enantiomer peaks of Example 14 were identical with the majorenantiomer peaks of Example 13.

EXAMPLE 15 SYNTHESIS OF OPTICALLY ACTIVE(S)-1-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)PENTYLAMINE N-MONOMETHYL Step (c),Dehydration and Condensation

At first, 6.56 g (22.00 mmol, 1 eq.) of 3,5-bis(trifluoromethyl)phenyln-butyl ketone, 3.40 g (28.06 mmol, 1.28 eq.) of (S)-1-phenylethylamine,and 0.30 g (2.20 mmol, 0.10 eq.) of zinc chloride were added to 100 mlof toluene. The resulting mixture was stirred for 101 hr under a heatedreflux condition, while water (by-product) was removed from a Dean-Starktrap. The resulting reaction liquid was washed with 5% sodium hydroxideaqueous solution and then 1.4N ammonium chloride aqueous solution. Therecovered organic layer was dried with anhydrous sodium sulfate,filtrated, concentrated and vacuum-dried, thereby obtaining 8.89 g of acrude product of an optically active imine represented by the followingformula.

The conversion was found by gas chromatography to be 98%. The molecularratio of E configuration to Z configuration of the crude product wasfound by ¹H-NMR to be 85:15.

¹H-NMR (TMS; CDCl₃) of E configuration, δppm: 0.92 (t, 8.0 Hz, 3H),1.28-1.50 (m, 4H), 1.55 (d, 6.7 Hz, 3H), 2.77 (t, 8.0 Hz, 2H), 4.91 (q,6.7 Hz, 1H), 7.10-7.55 (Ar—H, 5H), 7.88 (Ar—H, 1H), 8.26 (Ar—H, 2H).

¹H-NMR (standard substance: TMS; solvent: CDCl₃) of Z configuration,δppm: 0.92 (t, 8.0 Hz, 3H), 1.28-1.50 (m, 4H), 1.55 (d, 6.7 Hz, 3H),2.77 (t, 8.0 Hz, 2H), 4.17 (q, 6.7 Hz, 1H), 7.10-7.55 (Ar—H, 5H), 8.09(Ar—H, 1H), 8.51 (Ar—H, 2H).

Step (d), Asymmetric Reduction

At first, 8.89 g (22.00 mmol, 1 eq.) of the crude product of theoptically active imine produced by the above step (c) were added to 88ml of methanol. The resulting solution was cooled down to −20° C. Then,1.00 g (26.43 mmol, 1.20 eq.) of sodium borohydride were added, followedby stirring for 12 hr at from the same temperature to 0° C. After thereaction, 1N hydrochloric acid aqueous solution was added to decomposethe remaining sodium borohydride. Then, the reaction liquid was madebasic by adding 2N sodium hydroxide aqueous solution, followed byextraction with toluene. The collected organic layer was washed withsaturated brine, dried with anhydrous sodium sulfate, filtrated,concentrated, and vacuum-dried, thereby obtaining 8.99 g of a crudeproduct of an optically active secondary amine represented by thefollowing formula.

It was found by gas chromatography that conversion of the crude productwas 100% and that the ratio of a diastereomer of S—S configuration to adiastereomer of R—S configuration was 85:15.

¹H-NMR (TMS, CDCl₃) of S—S configuration, δppm: 0.82 (t, 7.0 Hz, 3H),0.95-1.15 (m, 1H), 1.10-1.32 (m, 3H), 1.28 (d, 8.0 Hz, 3H), 1.40-1.85(m, 2H), 1.68 (br, 1H), 3.35 (q, 8.0 Hz, 1H), 3.44 (t, 7.0 Hz, 1H), 7.13(Ar—H, 2H), 7.26 (Ar—H, 1H), 7.33 (Ar—H, 2H), 7.66 (Ar—H, 2H), 7.77(Ar—H, 1H).

¹H-NMR (TMS, CDCl₃) of R—S configuration, δppm: 0.86 (t, 7.0 Hz, 3H),0.95-1.15 (m, 1H), 1.10-1.32 (m, 3H), 1.37 (d, 8.0 Hz, 3H), 1.40-1.85(m, 2H), 1.68 (br, 1H), 3.68 (q, 8.0 Hz, 1H), 3.74 (t, 7.0 Hz, 1H), 7.17(Ar—H, 2H), 7.25 (Ar—H, 1H), 7.33 (Ar—H, 2H), 7.61 (Ar—H, 2H), 7.63(Ar—H, 1H).

Step (a), Alkylation

At first, 1.10 g (2.69 mmol, 1 eq.) of the above crude product of theoptically active secondary amine, 3.00 g (21.14 mmol, 7.86 eq.) ofmethyl iodide, and 0.75 g (5.43 mmol, 2.02 eq.) of anhydrous potassiumcarbonate were added to 5.0 ml of dimethylformainide, followed bystirring at room temperature for 43 hr. After the reaction, the reactionliquid was diluted with ethyl acetate, followed by washing with waterand saturated brine, drying with anhydrous sodium sulfate, filtration,concentration, and vacuum drying, thereby obtaining 1.99 g of a crudeproduct of an optically active tertiary amine represented by thefollowing formula.

Conversion was found by gas chromatography to be 95%. Furthermore, thecrude product was purified by a silica gel column chromatography (ethylacetate : n-hexane=1:50), thereby obtaining 0.89 g of a purified productof the optically active tertiary amine. The yield was 79%.

¹H-NMR (TMS, CDCl₃) of S—S configuration, δppm: 0.84 (t, 7.2 Hz, 3H),0.93-1.13 (m, 1H), 1.13-1.35 (m, 3H), 1.28 (d, 6.8 Hz, 3H), 1.59-1.78(m, 1H), 1.82-2.00 (m, 1H), 2.13 (s, 3H), 3.47 (q, 6.8 Hz, 1H), 3.73 (t,7.3 Hz, 1H), 7.21-7.42 (Ar—H, 5H), 7.61 (Ar—H, 2H), 7.77 (Ar—H, 1H).

¹H-NMR (TMS, CDCl₃) of R—S configuration, δppm: 0.85 (t, 7.3 Hz, 3H),0.93-1.13 (m, 1H), 1.13-1.35 (m, 3H), 1.32 (d, 6.8 Hz, 3H), 1.59-1.78(m, 1H), 1.82-2.00 (m, 1H), 2.12 (s, 3H), 3.66 (q, 6.8 Hz, 1H), 3.76 (t,7.3 Hz, 1H), 7.21-7.42 (Ar—H, 5H), 7.61 (Ar—H, 2H), 7.76 (Ar—H, 1H).

Step (b), Hydrogenolysis

To 1.4 ml of methanol, 0.57 g (1.37 mmol, 1 eq.) of the above purifiedproduct of the optically active tertiary amine and 10.0 mg (0.04 wt %Pd) of a palladium catalyst (having 5% palladium carried on an activatedcarbon containing 50 wt % of water) were added. The hydrogen pressurewas adjusted to 0.5 MPa, and the stirring was conducted at 60° C. for 14hr. After the reaction, the reaction liquid was filtrated using afiltration aid (CELITE (trade name)), concentrated, and vacuum-dried,thereby obtaining 0.42 g of a crude product of an optically active(S)-1-(3,5-bis(trifluoromethyl)phenyl)pentylamine N-monomethyl,represented by the following formula.

The yield was 98%. The above crude product was found by chiral gaschromatography to have a conversion of 100% and an enantiomeric excessof 70% ee. In terms of severing position selectivity whether the N—C*bond is severed at the broken line “a” to produce a compound A or at thebroken line “b” to produce a compound B (i.e., the above opticallyactive (S)-1-(3,5-bis(trifluoromethyl)phenyl)pentylamine N-monomethyl)in the above formula 11, the above crude product was found by chiral gaschromatography to contain 1 part by mole of the compound A and 99 partsby mole of the compound B.

¹H-NMR (TMS, CDCl₃), δppm: 0.86 (t, 7.2 Hz, 3H), 1.04-1.18 (m, 1H),1.18-1.37 (m, 3H), 1.55-1.68 (m, 1H), 1.68-1.82 (m, 1H), 2.26 (s, 3H),2.60 (br, 1H), 3.60 (t, 7.2 Hz, 1H), 7.76 (Ar—H, 2H), 7.78 (Ar—H, 1H).

EXAMPLE 16 SYNTHESIS OF OPTICALLY ACTIVE (R)-1-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)PENTYLAMINE N-MONOMETHYL

Example 15 was repeated except in that (S)-1-phenylethylamine wasreplaced in the step (c) with (R)-1-phenylethylamine, thereby obtainingan optically active (R)-1-(3,5-bis(trifluoromethyl)phenyl)pentylamineN-monomethyl.

NMR data of an optically active tertiary amine, represented by thefollowing formula, are shown as follows.

¹H-NMR (TMS, CDCl₃) of R—R configuration, δppm: 0.84 (t, 7.2 Hz, 3H),0.93-1.13 (m, 1H), 1.13-1.35 (m, 3H), 1.28 (d, 6.8 Hz, 3H), 1.59-1.78(m, 1H), 1.82-2.00 (m, 1H), 2.13 (s, 3H), 3.47 (q, 6.8 Hz, 1H), 3.73 (t,7.3 Hz, 1H), 7.21-7.42 (Ar—H, 5H), 7.61 (Ar—H, 2H), 7.77 (Ar—H, 1H).

¹H-NMR (TMS, CDCl₃) of S—R configuration, δppm: 0.85 (t, 7.3 Hz, 3H),0.93-1.13 (m, 1H), 1.13-1.35 (m, 3H), 1.32 (d, 6.8 Hz, 3H), 1.59-1.78(m, 1H), 1.82-2.00 (m, 1H), 2.12 (s, 3H), 3.66 (q, 6.8 Hz, 1H), 3.76 (t,7.3 Hz, 1H), 7.21-7.42 (Ar—H, 5H), 7.61 (Ar—H, 2H), 7.76 (Ar—H, 1H).

NMR data of an optically active(R)-1-(3,5-bis(trifluoromethyl)phenyl)pentylamine N-monomethyl,represented by the following formula, are shown as follows.

¹H-NMR (TMS, CDCl₃), δppm: 0.86 (t, 7.2 Hz, 3H), 1.04-1.18 (m, 1H),1.18-1.37 (m, 3H), 1.55-1.68 (m, 1H), 1.68-1.82 (m, 1H), 2.26 (s, 3H),2.60 (br, 1H), 3.60 (t, 7.2 Hz, 1H), 7.76 (Ar—H, 2H), 7.78 (Ar—H, 1H).

In chiral gas chromatography, the major enantiomer peaks of Example 16were identical with the minor enantiomer peaks of Example 15, and theminor enantiomer peaks of Example 16 were identical with the majorenantiomer peaks of Example 15.

EXAMPLE 17 SYNTHESIS OF OPTICALLY ACTIVE(S)-1-(4-TRIFLUOROMETHOXYPHENYL)ETHYLAMINE N-MONOMETHYL Step (c),Dehydration and Condensation

At first, 5.00 g (24.49 mmol, 1 eq.) of 4-trifluoromethoxyphenyl methylketone, 3.26 g (26.90 mmol, 1.10 eq.) of (S)-1-phenylethylamine, and0.23 g (1.69 mmol, 0.07 eq.) of zinc chloride were added to 24.5 ml oftoluene. The resulting mixture was stirred for 22 hr under a heatedreflux condition, while water (by-product) was removed from a Dean-Starktrap. The resulting reaction liquid was washed with 1.5% sodiumhydroxide aqueous solution and then 1.5N ammonium chloride aqueoussolution. The recovered organic layer was concentrated and vacuum-dried,thereby obtaining 7.61 g of a crude product of an optically active iminerepresented by the following formula.

The conversion was found by gas chromatography to be 96%.

¹H-NMR (TMS; CDCl₃), δppm: 1.53 (d, 6.8 Hz, 3H), 2.27 (s, 3H), 4.83 (q,6.8 Hz, 1H), 7.22 (Ar—H, 2H), 7.23 (Ar—H, 1H), 7.33 (Ar—H, 2H), 7.45(Ar—H, 2H), 7.88 (Ar—H, 2H).

Step (d), Asymmetric Reduction

At first, 7.61 g (24.49 mmol, 1 eq.) of the crude product of theoptically active imine produced by the above step (c) were added to 18.7ml of methanol. The resulting solution was cooled down to −5° C. Then,0.93 g (24.58 mmol, 1.00 eq.) of sodium borohydride were added, followedby stirring for 2 hr at the same temperature. After the reaction, 1Nhydrochloric acid aqueous solution was added to decompose the remainingsodium borohydride. Then, the reaction liquid was made basic by adding3N sodium hydroxide aqueous solution, followed by extraction withtoluene. The collected organic layer was washed with saturated brine,dried with anhydrous sodium sulfate, filtrated, concentrated, andvacuum-dried, thereby obtaining 7.66 g of a crude product of anoptically active secondary amine represented by the following formula.

It was found by gas chromatography that conversion of the crude productwas 100% and that the ratio of a diastereomer of S—S configuration to adiastereomer of R—S configuration was 85:15.

¹H-NMR (TMS, CDCl₃) of S—S configuration, δppm: 1.24 (d, 6.8 Hz, 3H),1.27 (d, 6.8 Hz, 3H), 1.55 (br, 1H), 3.46 (q, 6.8 Hz, 1H), 3.52 (q, 6.8Hz, 1H), 7.09-7.37 (Ar—H, 9H).

¹H-NMR (TMS, CDCl₃) of R—S configuration, δppm: 1.33 (d, 6.4 Hz, 3H),1.35 (d, 6.4 Hz, 3H), 1.55 (br, 1H), 3.76 (q, 6.4 Hz, 2H), 7.09-7.37(Ar—H, 9H)

Step (a), Alkylation

At first, 3.50 g (11.19 mmol, 1 eq.) of the above crude product of theoptically active secondary amine, 2.49 g (22.61 mmol, 2.02 eq.) ofmethyl methanesulfonate, and 2.42 g (22.59 mmol, 2.02 eq.) of2,6-lutidine were added to a mixed solution of 1.0 ml ofdimethylformamide and 10.2 ml of tetrahydrofuran, followed by stirringat 60° C. for 16 hr. After the reaction, the reaction liquid wasfiltrated using a filtration aid (CELITE (trade name)), followed bydilution with toluene, washing with saturated sodium hydrogencarbonateand saturated brine, drying with anhydrous sodium sulfate, filtration,concentration, and vacuum drying, thereby obtaining 3.93 g of a crudeproduct of an optically active tertiary amine represented by thefollowing formula.

Conversion was found by gas chromatography to be 95%. Furthermore, thecrude product was purified by a silica gel column chromatography (ethylacetate : n-hexane=1:20), thereby obtaining 3.04 g of a purified productof the optically active tertiary amine. The total yield from thedehydration and the condensation to the alkylation was 84%.

¹H-NMR (TMS, CDCl₃) of S—S configuration, δppm: 1.32 (d, 6.8 Hz, 3H),1.34 (d, 6.8 Hz, 3H), 1.98 (s, 3H), 3.80 (q, 6.8 Hz, 1H), 3.85 (q, 6.8Hz, 1H), 7.10-7.46 (Ar—H, 9H).

Step (b), Hydrogenolysis

To 3.0 ml of methanol, 0.97 g (3.00 mmol, 1 eq.) of the above purifiedproduct of the optically active tertiary amine, 0.90 g (14.99 mmol, 5.00eq.) of acetic acid and 48.5 mg (0.125 wt % Pd) of a palladium catalyst(having 5% palladium carried on an activated carbon containing 50 wt %of water) were added. The hydrogen pressure was adjusted to 0.5 MPa, andthe stirring was conducted at 60° C. for 16 hr. After the reaction, thereaction liquid was filtrated using a filtration aid (CELITE (tradename)), concentrated, and vacuum-dried, thereby obtaining a crudeproduct of an acetate of an optically active(S)-1-(4-trifluoromethoxyphenyl)ethylamine N-monomethyl, represented bythe following formula.

Then, 1N sodium hydroxide aqueous solution was added to the above crudeproduct of the acetate to have a basic solution, followed by extractionwith ethyl acetate. The recovered organic layer was dried with anhydroussodium sulfate, followed by filtration, concentration and vacuum drying,thereby obtaining 0.59 g of a crude product of an optically active(S)-1-(4-trifluoromethoxyphenyl)ethylamine N-monomethyl, represented bythe following formula.

The yield was 89%. The above crude product was found by chiral gaschromatography to have a conversion of 100% and an enantiomeric excessof 70% ee. In terms of severing position selectivity whether the N—C*bond is severed at the broken line “a” to produce a compound A or at thebroken line “b” to produce a compound B (i.e., the above opticallyactive (S)-1-(4-trifluoromethoxyphenyl)ethylamine N-monomethyl) in theabove formula 11, the above crude product was found by chiral gaschromatography to contain 1 part by mole of the compound A and 99 partsby mole of the compound B.

¹H-NMR (TMS, CDCl₃), δppm: 1.34 (d, 6.8 Hz, 3H), 1.63 (br, 1H), 2.30 (s,3H), 3.67 (q, 6.8 Hz, 1H), 7.17 (Ar—H, 2H), 7.33 (Ar—H, 2H).

EXAMPLE 18 SYNTHESIS OF OPTICALLY ACTIVE(R)-1-(4-TRIFLUOROMETHOXYPHENYL)ETHYLAMINE N-MONOMETHYL

Example 17 was repeated except in that (S)-1-phenylethylamine wasreplaced in the step (c) with (R)-1-phenylethylamine, thereby obtainingan optically active (R)-1-(4-trifluoromethoxyphenyl)ethylamineN-monomethyl.

NMR data of an optically active tertiary amine, represented by thefollowing formula, are shown as follows.

¹H-NMR (TMS, CDCl₃) of R—R configuration, δppm: 1.32 (d, 6.8 Hz, 3H),1.34 (d, 6.8 Hz, 3H), 1.98 (s, 3H), 3.80 (q, 6.8 Hz, 1H), 3.85 (q, 6.8Hz, 1H), 7.10-7.46 (Ar—H, 9H).

NMR data of an optically active(R)-1-(4-trifluoromethoxyphenyl)ethylamine N-monomethyl, represented bythe following formula, are shown as follows.

¹H-NMR (TMS, CDCl₃), δppm: 1.34 (d, 6.8 Hz, 3H), 1.63 (br, 1H), 2.30 (s,3H), 3.67 (q, 6.8 Hz, 1H), 7.17 (Ar—H, 2H), 7.33 (Ar—H, 2H).

In chiral gas chromatography, the major enantiomer peaks of Example 18were identical with the minor enantiomer peaks of Example 17, and theminor enantiomer peaks of Example 18 were identical with the majorenantiomer peaks of Example 17.

The entire contents of Japanese Patent Application No. 2002-261148(filed Sep. 6, 2002), which is a basic Japanese application of thepresent application, are incorporated herein by reference.

1. An optically active tertiary amine represented by the formula 3,

wherein R represents a fluorine atom, trifluoromethyl group ortrifluoromethoxy group, n represents an integer of from 1 to 5, each ofR¹ and R² independently represents an alkyl group having a carbon atomnumber of from 1 to 6, Me represents a methyl group, Ar represents aphenyl group or 1- or 2-naphthyl group, and * represents a chiralcarbon.
 2. An optically active 1-(fluoro-substituted phenyl)alkylamineN-monoalkyl derivative represented by the formula 8,

wherein n represents an integer of from 1 to 5, each of R¹ and R²independently represents an alkyl group having a carbon atom number offrom 1 to 6, and * represents a chiral carbon.
 3. An optically active1-(trifluoromethyl-substituted phenyl)alkylamine N-monoalkyl derivativerepresented by the formula 9,

wherein n represents an integer of from 1 to 5, each of R¹ and R²independently represents an alkyl group having a carbon atom number offrom 1 to 6, * represents a chiral carbon, and the N-monoalkylderivative is a compound except an optically active1-(3,5-bis(trifluoromethyl)phenyl)ethylamine N-monomethyl.
 4. Anoptically active 1-(trifluoromethoxy-substituted phenyl)alkylamineN-monoalkyl derivative represented by the formula 10,

wherein n represents an integer of from 1 to 5, each of R¹ and R²independently represents an alkyl group having a carbon atom number offrom 1 to 6, and * represents a chiral carbon.